| Food | HEALTH ALERT | Various Meat and Poultry Products Containing FDA-Regulated recalled | FSIS | Salmonella | |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Arthrogram Tray recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Viper¿ 3-Stage Fixed Wire Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Medline Kits: D AND C PACK recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Headhunter , Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus recalled | Xtant Medical Holdings | Labeling Errors | Nationwide |
| Device | CLASS II | Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Oxoid Agglutinating Sera, Salmonella 9-0 R30957301 recalled | Remel Europe | Salmonella | Nationwide |
| Device | CLASS II | Medline Kits: Angio Cath Pack-mary Immaculat recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Sequencing Agent SEQ0067, component of FoundationOne CDx (F1CDx) recalled | Foundation Medicine | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Arrowg+ard Blue¿ MAC" Two-Lumen Central Venous Access Kit recalled | Arrow International | Other | Nationwide |
| Device | CLASS II | Custom Convenience Kits Pre Op Kit - NS recalled | Windstone Medical Packaging | Other | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Arrow Echogenic Introducer Needle recalled by Arrow International | Arrow International | Other | Nationwide |
| Device | CLASS II | AccuVu Angiographic Catheter, Omni Flush, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Kits: PICC Tray recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Sos Omni Selective , Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | The product is a handheld ultraviolet-C germicidal wand recalled | Uvlizer c/o Rais International | Other | DE |
| Device | CLASS II | Flamingo Funnel Large recalled by SurgiSmoke Solutions | SurgiSmoke Solutions | Sterility | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Straight Art, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | The product is a handheld ultraviolet-C germicidal wand recalled | Uvlizer c/o Rais International | Other | DE |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Infant Central Line Dressing Change Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Syr Control Rotating recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat II Shears w/Ultrasonic Mode recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Viper¿ 3-Stage Wire Guided Balloon Dilator recalled | Diversatek Healthcare | Other | 19 states |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Kits: Gyn Laparoscopy Pack recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Syringes: Syringe Control W/Rotator recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Newborn Admission recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Kits: Bwnboro Craniotomy Pack-lf recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat II Shears w/Ultrasonic Mode recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | Medline Kits: Arthroscopy Pack recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Pigtail, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Pressure Injectable Arrowg+ard Blue Plus¿ Four-Lumen CVC Kit recalled | Arrow International | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | IV Start Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | AccuVu Angiographic Catheter, Pigtail, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Avitene Ultrafoam Microfibrillar Collagen Hemostat recalled by Davol | Davol | Foreign Material | Nationwide |
| Device | CLASS II | Flamingo Funnel Medium recalled by SurgiSmoke Solutions | SurgiSmoke Solutions | Sterility | Nationwide |
| Device | CLASS II | Central Line Dressing Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Kits: General Laparoscopy recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Syr Cntrl Ring W/Rot NB recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Standard Central Line Dressing Change Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Custom Convenience Kits Pre Op Kit - NS recalled | Windstone Medical Packaging | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Kits: Labor Pack-22025208-LF recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | LeadCare Ultra Blood Lead Test Kit recalled by Magellan Diagnostics | Magellan Diagnostics | Device Malfunction | Nationwide |
| Device | CLASS II | CUSA Clarity C7000 Console recalled by Integra LifeSciences Corp. | Integra LifeSciences Corp. (NeuroSciences) | Device Malfunction | Nationwide |
| Device | CLASS II | Percutaneous Sheath Introducer with 7.5 -. Catheter recalled | Arrow International | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Cobra , Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Flextip Plus Epidural Catheter;flexblock Continous recalled | Arrow International | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Berenstein, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Protocol Configuration Tool (PCT) recalled by Foundation Medicine | Foundation Medicine | Device Malfunction | MA, NC |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Omni Flush, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Kits: Breast Pack recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Namic Syringes: Syr Cntrl Ring W/Rot NB recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Arrow, Arrowg+ard And Arrowg+ard Blue Plus Pressure recalled | Arrow International | Other | Nationwide |
| Device | CLASS II | Arrow Radial Artery Catheterization Kit recalled by Arrow International | Arrow International | Other | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Access Total T4 Calibrator recalled by Beckman Coulter | Beckman Coulter | Other | Nationwide |
| Device | CLASS II | (2) LeadCare¿ II Blood Lead Test Kit recalled by Magellan Diagnostics | Magellan Diagnostics | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Rover Mobile X-ray System recalled by Micro-X | Micro-X | Device Malfunction | Nationwide |
| Device | CLASS II | Custom Convenience Kits Pre Op Kit - NS recalled | Windstone Medical Packaging | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: ENT PACK recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Flamingo Funnel Small recalled by SurgiSmoke Solutions | SurgiSmoke Solutions | Sterility | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Medline Kits: Mts Left Heart Kit-carolinas Hos recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Hysteroscopy Pack recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Pigtail, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | LeadCare¿ Plus Blood Lead Test Kit recalled by Magellan Diagnostics | Magellan Diagnostics | Packaging Defects | Nationwide |
| Device | CLASS II | AccuVu Angiographic Catheter, Omni Flush, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | MAC" Two-Lumen Central Venous Access Kit for use recalled | Arrow International | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat II Shears w/Ultrasonic Mode recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Foley Urine Collection Kit recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Berenstein, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Angiography Pack-lf recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: CATH LAB CDS recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Wound Closure Tray recalled by LSL Healthcare | LSL Healthcare | Sterility | Nationwide |
| Device | CLASS II | Oer-elite Endoscope Reprocessor Connecting Tubes recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | AccuVu Angiographic Catheter, Straight Flush, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Namic Guidewires: Guidewire 3MMJ 0.035X260CM LT recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus Thunderbeat II Shears w/Ultrasonic Mode recalled | Olympus Corporation of the Americas | Other | PA |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits containing select SKUs recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline Kits: Heart Transplant Biopsy recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Soft-Vu Angiographic Catheter, Kumpe, Non-Braided recalled | Angiodynamics | Device Malfunction | Nationwide |
| Drug | CLASS II | Pantoprazole Sodium, Delayed-Release Tablets, USP, 40 mg recalledPantoprazole Sodium | Hetero Labs Limited (Unit V) | Other | Nationwide |
| Drug | CLASS II | Sterile Water for Injection recalled by B Braun MedicalSterile Water | B Braun Medical | Sterility | Nationwide |
| Drug | CLASS II | 0.9 % Sodium Chloride Irrigation recalled by B Braun MedicalSodium Chloride For Irrigation | B Braun Medical | Sterility | Nationwide |
| Drug | CLASS II | Claravis (isotretinoin capsule, USP), 10 mg, Packaged as a) recalledClaravis | Teva Pharmaceuticals USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Lactated Ringer's Irrigation, Sterile, Ex only recalledLactated Ringers Irrigation | B Braun Medical | Sterility | Nationwide |
| Drug | CLASS III | Premier, Monsel's, Ferric Subsulfate Solution recalledMonsels Solution | Premier Dental Products | Other | Nationwide |
| Drug | CLASS II | Furosemide Tablets, USP, 80 mg recalled by Leading PharmaFurosemide | Leading Pharma | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Dextrose Injection recalled by B Braun MedicalDextrose | B Braun Medical | Sterility | Nationwide |
| Drug | CLASS II | Freshkote Lubricant Eyedrops, Sterile, Harrow Eye Llc recalled | Harrow Eye | Sterility | Nationwide |
| Drug | CLASS II | Omega-3-Acid, Ethyl Esters, Capsules recalled by The Harvard Drug GroupOmega-3-acid Ethyl Esters | The Harvard Drug Group | Potency & Assay | Nationwide |
| Food | CLASS II | Chips Ahoy! Baked Bites Brookie . Carton ( pouch ) recalled | Mondelez Global | Other | 11 states |
| Food | CLASS II | EL Mexicano horchata casera Instant Horchata Drink recalledEL Mexicano | Marquez Brothers International | Undeclared Milk | 29 states |
| Food | CLASS II | EL Mexicano agua fresca de horchata Instant Horchata Drink recalledEL Mexicano | Marquez Brothers International | Undeclared Milk | 29 states |
| Food | CLASS I | Salute Seasonings recalled by Unistel IndustriesSalute Seasonings | Unistel Industries | Salmonella | CA, HI, WA |
| Food | CLASS II | Bulk Horchata Powder 3951 (100547) 1/25 Horchata recalledBulk Horchata | Marquez Brothers International | Undeclared Milk | 29 states |
| Food | CLASS II | Bombay Kitchen Punjabi Mix recalled by Ethnic FoodsBombay | Ethnic Foods | Undeclared Allergens | NJ |
| Food | CLASS II | Spice Powder, Plastic recalled by Summit Import | Summit Import | Lead & Heavy Metals | 8 states |
| Food | CLASS I | Kirkland Signature Traditional Madeleines recalled by Costco WholesaleKirkland Signature | Costco Wholesale | Undeclared Tree Nuts | 9 states |
| Food | CLASS II | Bombay Kitchen Tikka Sev recalled by Ethnic FoodsBombay | Ethnic Foods | Undeclared Allergens | NJ |
| Device | CLASS I | B. Braun Hemodialysis Bloodlines recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS I | B. Braun Hemodialysis Bloodlines, Low Vol, NO Chamber Pump Segment recalled | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Cytal Wound Matrix 2-Layer cm. Product ID: WSM1015 recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | Cytal Wound Matrix 2-Layer cm. Product ID: WSM0710 recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS I | B Braun Hemodialysis Bloodlines, Low Vol, NO Chamber Pump Segment recalled | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Core Workstation, a component of the Core Shoulder System recalled | Linkbio | Other | Nationwide |
| Device | CLASS II | Cytal Burn Matrix cm. Product ID: BMM0710 recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS I | B. Braun Hemodialysis Bloodlines, Streamline Fresenius For Davita recalled | B Braun Medical | Other | Nationwide |
| Device | CLASS I | B. Braun Hemodialysis Bloodlines recalled by B Braun Medical | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Centurion Circumcision Kit, Medline Kit Number recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Artis Pheno VE30A and VE40A recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | PA |
| Device | CLASS II | Philips Spectral CT on Rails recalled by Philips Medical Systems | Philips Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS I | B. Barun Hemodialysis Bloodlines, StreamLine Bloodline Long recalled | B Braun Medical | Other | Nationwide |
| Device | CLASS II | Cytal Wound Matrix 2-Layer cm. Product ID: WSM0505 recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | Elegance¿ Anterior Cervical Plate Elegance 1 Level recalled | Clariance-SAS | Device Malfunction | Nationwide |
| Device | CLASS II | iLet Ace Pump Kit recalled by Beta Bionics | Beta Bionics | Device Malfunction | Nationwide |
| Device | CLASS II | Philips AneurysmFlow recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Cellex Photopheresis System Cellex Photopheresis Kit recalled | Therakos Development | Device Malfunction | Nationwide |
| Device | CLASS II | Instinct Plus Endoscopic Clipping Device recalled by Wilson-Cook Medical | Wilson-Cook Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Cytal Burn Matrix cm. Product ID: BMM1015 recalled | Integra LifeSciences Corp. (NeuroSciences) | Other | Nationwide |
| Device | CLASS II | Hf-oct Imaging System recalled by Gentuity | Gentuity | Device Malfunction | Nationwide |
| Device | CLASS II | Yeastone Broth, 10/BOX YY3462 recalled by Remel | Remel | Other | Nationwide |
| Device | CLASS I | Omnipod 5 Pods recalled by Insulet | Insulet | Packaging Defects | Nationwide |
| Device | CLASS II | Arjo Tenor mobile passive patient lift recalled | Arjohuntleigh Polska Sp. z.o.o | Device Malfunction | Nationwide |
| Device | CLASS II | React Health Phoenix Oxygen Concentrator recalled by 3B Medical | 3B Medical | Other | Nationwide |
| Drug | CLASS II | QC Quality Choice, Menthol- Cough Suppressant Oral recalledQuality Choice | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Lidocaine HCl Injection, USP, 2%, 100 mg recalled by Huons CoLidocaine Hydrochloride | Huons | Sterility | Nationwide |
| Drug | CLASS II | MGC Health, Menthol- Cough Suppressant, Oral Anesthetic recalledMgc Health | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Blemish Spot Treatment (Salicylic Acid) 1%, ., Skin Script recalled | Island Kinetics, Inc. d.b.a. CoValence Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | HydroPeptide Clear Alliance Serum, 2.5% Benzoyl Peroxide, a) recalled | Owen Biosciences | Benzene | Nationwide |
| Drug | CLASS II | QC Quality Choice, Menthol-Cough Suppressant Oral recalledQuality Choice | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Lidocaine HCl injection, USP, 1% 50mg/ (10 mg/mL) Single Dose Vials recalledLidocaine Hydrochloride | Huons | Sterility | Nationwide |
| Drug | CLASS III | Magnesium Chloride, 6-Hydrate, Crystal recalled | Avantor Performance Materials | Potency & Assay | Nationwide |
| Drug | CLASS II | Bupivacaine Hydrochloride 0.75% in 8.25% Dextrose Injection recalledBupivacaine Hydrochloride | Huons | Sterility | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 60 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS III | Skin Rehab, Calming Skin Gel, Hydrocortisone Balm, hydrocortisone recalled | Island Kinetics, Inc. d.b.a. CoValence Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP Ampules recalled by Huons CoSodium Chloride | Huons | Sterility | Nationwide |
| Drug | CLASS II | caring mill, Menthol Cough Suppressant Oral Anesthetic recalledCaring Mill Cough Drops Cherry | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Slmd Benzoyl Peroxide Acne Lotion, Benzoyl Peroxide recalled | Owen Biosciences | Benzene | Nationwide |
| Drug | CLASS II | QC Quality Choice, Menthol-Cough Suppressant Oral recalledQuality Choice Cough Drops Vanilla Honey | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | exchange select, Menthol- Cough Suppressant Oral Anesthetic recalledMenthol Flavor Cough Drop | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | QC Quality Choice, Pectin Oral Demulcent recalledQuality Choice Cough Drops Creamy Strawberry | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | QC Quality Choice, Menthol- Cough Suppressant Oral recalledQuality Choice | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Memantine Hydrochloride Extended-Release, Capsules, 7 mg recalledMemantine Hydrochloride | The Harvard Drug Group | Potency & Assay | Nationwide |
| Drug | CLASS II | QC Quality Choice, Menthol-Cough Suppressant Oral recalledQuality Choice | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Fluocinonide, USP, 0.05% Cream tube recalledFluocinonide | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS II | Discount Drug Mart Food Market, Cough Drops recalledDiscount Drug Mart | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Albuterol Sulfate Inhalation Solution, 0.5%, 25 mg recalled | Nephron SC | Other | Nationwide |
| Drug | CLASS II | QC Quality Choice, Menthol-Cough Suppressant Oral recalledQuality Choice | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 90 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Fluocinonide, USP, 0.05% Cream tube recalledFluocinonide | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS III | Essential Calming Skin Gel, hydrocortisone recalled | Island Kinetics, Inc. d.b.a. CoValence Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | SLMD BP Acne Spot Treatment, 10% Benzoyl Peroxide -, Sandra Lee MD recalled | Owen Biosciences | Benzene | Nationwide |
| Drug | CLASS II | Epinephrine Injection, USP, 1 mg/ (0.1 mg/mL) recalledEpinephrine | International Medication Systems | Sterility | Nationwide |
| Drug | CLASS II | Desmopressin Nasal Spray, USP, 10 mcg/ bottle (50 doses) recalled | Apotex | Other | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 30 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Semaglutide-Glycine-Cyanocobalamin Injectable, 2.5 mg, 5 mg recalled | Payless Compounders | Sterility | OR |
| Drug | CLASS III | Remedy Gel, hydrocortisone 1% recalled by Island Kinetics, Inc. d.b.a. | Island Kinetics, Inc. d.b.a. CoValence Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | exchange select, Menthol -Cough Suppressant Oral Anesthetic recalledHoney Lemon Flavor Cough Drop | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Discount Drug Mart Food Market, Cough Drops recalledDiscount Drug Mart | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | MGC Health, Menthol- Cough Suppressant, Oral Anesthetic recalledMgc Health | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Fhf Farmhouse Fresh, Midnight Clearing, Night Lotion recalled | Owen Biosciences | Benzene | Nationwide |
| Drug | CLASS II | MGC Health, Menthol- Cough Suppressant, Oral Anesthetic recalledMgc Health | Xiamen Kang Zhongyuan Biotechnology | Processing Deviation | Nationwide |
| Drug | CLASS II | Fluocinonide, USP, 0.05% Cream tube recalledFluocinonide | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Food | CLASS II | Label is predominantly green with white lettering in a container recalledLabel | Pure Palm C/o Dvd | Labeling Errors | 5 states |
| Food | CLASS III | Raw & Unfiltered Bee Well Wildflower Honey recalled | Bee Well Honey Farm & Supply | Other | SC |
| Food | CLASS II | Booey's Dragon's Breath sauce ringneck recalled by Booey's GourmetBooey's Dragon's | Booey's Gourmet | Undeclared Fish & Shellfish | WA |
| Device | CLASS II | MicroScan Neg Multidrug Resistant MIC recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | CA |
| Device | CLASS II | Multi-parameter Command Module recalled by Spacelabs Healthcare | Spacelabs Healthcare | Labeling Errors | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medical Cook Staged Extubation Set: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Medical Cook¿ Spectrum¿ Central Venous Catheter Tray: Reference recalled | Cook | Other | IN |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medical Wayne Pneumothorax Tray: Reference recalled by Cook Incorporated | Cook | Other | IN |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medical Approach Cto-12 Micro Wire Guide: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Medical NCompass¿ Nitinol Stone Extractor: Reference recalled | Cook | Other | IN |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medical Ciaglia Blue Rhino Percutaneous Tracheostomy recalled | Cook | Other | IN |
| Device | CLASS II | Medical Multipurpose Drainage Catheter: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Medical Blue Rhino G2-Multi Percutaneous Tracheostomy recalled | Cook | Other | IN |
| Device | CLASS II | HRS Max parts: Tornier HRS Max Tuberosity Body Lat Coat, Small recalled | Tornier | Labeling Errors | Nationwide |
| Device | CLASS II | See Luer Cap Set, MPC-130, set, administration, intravascular recalled | Molded Products | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | MicroScan Neg MIC 3J recalled by Beckman Coulter | Beckman Coulter | Other | CA |
| Device | CLASS II | Medical Thal-Quick Chest Tube Tray: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Medical Approach Cto-6 Micro Wire Guide, Reference recalled | Cook | Other | IN |
| Device | CLASS II | Medical Spectrum¿ Central Venous Catheter Set: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Artis pheno and Artis Icono biplane, floor and ceiling recalled | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | Medical Spectrum¿ Central Venous Tray: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder recalled | Stryker Sustainability Solutions | Other | 41 states |
| Device | CLASS II | B¿R¿A¿H¿M¿S Kryptor compact React recalled | Brahms | Potency & Assay | 15 states |
| Device | CLASS II | Medical Approach Cto-18 Micro Wire Guide, Reference recalled | Cook | Other | IN |
| Device | CLASS I | Namic Angiographic Syringe, labeled as follows recalled | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medical Blue Rhino¿ G2-Multi Percutaneous Tracheostomy recalled | Cook | Other | IN |
| Device | CLASS II | Medical Wayne Pneumothorax Set: Reference recalled by Cook Incorporated | Cook | Other | IN |
| Device | CLASS II | Medical Cook¿ Strange Bile Duct Stone Exploration Set: Reference recalled | Cook | Other | IN |
| Device | CLASS II | Melker Universal Cuffed Emergency Cricothyrotomy Catheter recalled | Cook | Other | IN |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS I | Namic Angiographic Control Syringe, labeled as follows recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medical Arterial Pressure Monitoring Tray, Reference recalled | Cook | Other | IN |
| Device | CLASS I | Medline medical convenience kits recalled by Medline Industries | Medline Industries | Other | Nationwide |
| Device | CLASS II | Xtant Medical Xpress Pedicle Screw System Dual Lead recalled | Xtant Medical Holdings | Labeling Errors | OR |
| Drug | CLASS II | Lanreotide Injection, 120 mg* recalled by Cipla USALanreotide Acetate | Cipla USA | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP 900 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | Isotretinoin Capsules, USP, 30 mg recalled by Teva Pharmaceuticals USAIsotretinoin | Teva Pharmaceuticals USA | Potency & Assay | 4 states |
| Drug | CLASS II | GE Healthcare Omnipaque (iohexol) Injection, 300 mg/mL (64.7%) recalledOmnipaque | GE Healthcare Irel | Particulate Matter | Nationwide |
| Drug | CLASS II | Vancomycin HCL added to, 0.9% Sodium Chloride Injection recalled | Fagron Compounding Services | Sterility | Nationwide |
| Drug | CLASS II | Isotretinoin Capsules, USP, 40 mg Prescription Pacs recalledIsotretinoin | Teva Pharmaceuticals USA | Potency & Assay | 4 states |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP, 900 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP x60, Becton, Dickson recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP 0.9% (450 mg per (9 mg per mL) recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | norepinephrine Bitartrate,16mg per 0.9% Sodium Chloride recalled | Fagron Compounding Services | Sterility | Nationwide |
| Drug | CLASS II | Artificial Tears Lubricant Eye Drops (glycerin recalledArtificial Tears | Preferred Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Xanax XR, alprazolam, extended-release tablets, 3 mg recalled by ViatrisXanax | Viatris | Potency & Assay | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP, 900 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 5% Dextrose Injection, USP per (50 mg per mL) in a freeflex recalledDextrose | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 5% Dextrose Injection, USP per (50 mg per mL) in a freeflex recalledDextrose | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | norepinephrine Bitartrate, 32mg per 0.9% Sodium Chloride recalled | Fagron Compounding Services | Sterility | Nationwide |
| Drug | CLASS II | Clonidine Transdermal System, USP, 0.3 mg/day, supplied recalledClonidine Transdermal System | Teva Pharmaceuticals USA | Manufacturing (CGMP) Deviations | NJ |
| Drug | CLASS II | 5% Dextrose Injection, USP per (50 mg per mL) in a freeflex recalledDextrose | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | Lanreotide Injection, 120 mg recalled by Cipla USALanreotide Acetate | Cipla USA | Sterility | Nationwide |
| Drug | CLASS II | GE Healthcare Omnipaque (iohexol) Injection, 350 mg/mL (64.7%) recalledOmnipaque | GE Healthcare Irel | Particulate Matter | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP, 900 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | Vancomycin HCI added to, 0.9% Sodium Chloride Injection recalled | Fagron Compounding Services | Sterility | Nationwide |
| Drug | CLASS II | Clonidine Transdermal System, USP, 0.1 mg/day, supplied recalledClonidine Transdermal System | Teva Pharmaceuticals USA | Manufacturing (CGMP) Deviations | NJ |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP, (4,500 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP, 0.9% (900 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP 900 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | Clonidine Transdermal System, USP, 0.2 mg/day, supplied recalledClonidine Transdermal System | Teva Pharmaceuticals USA | Manufacturing (CGMP) Deviations | NJ |
| Drug | CLASS II | 0.45% Sodium Chloride Injection, USP per (4.5 mg per mL) recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium Chloride Injection, USP, (2,250 mg recalledSodium Chloride | Fresenius Kabi USA | Sterility | Nationwide |
| Drug | CLASS II | Vancomycin HCI added to, 0.9% Sodium Chloride Injection recalled | Fagron Compounding Services | Sterility | Nationwide |
| Food | CLASS II | Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids recalledVital Nutrients | Blueroot Health | Undeclared Egg | 40 states |
| Food | CLASS II | ReadyMeals Turkey Bacon & Cheddar Pretzel Duo Sandwich recalledReadyMeals | F&S Fresh Foods | Undeclared Sesame | OR |
| Food | CLASS I | Boner Bears Honey Male Enhancement 100% Wildflower Honey recalledBoner Bears | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |
| Food | CLASS II | Zarlengo's Chocolate Gelato recalled by Zarlengo Italian IceZarlengo's | Zarlengo Italian Ice | Undeclared Allergens | IL, IN, TX |
| Food | CLASS I | Fresh Cantaloupe (Whole, Fresh), brand name Ayco, wrapped recalled | Ayco Farms | Salmonella | 4 states |
| Food | CLASS III | Olive Skewers individually wrapped recalled by Mei Yu Cheng Da TradingOlive Skewers | Mei Yu Cheng Da Trading | Hidden Drug Ingredients | FL, NY, PA |
| Food | CLASS I | Red Bull Extreme Male Enhancement Supplement recalled | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |
| Food | CLASS III | Dadi Nongfu Dried Salt Chilli Vegetable(s) recalledDadi Nongfu | Mei Yu Cheng Da Trading | Hidden Drug Ingredients | FL, NY, PA |
| Food | CLASS I | Blue Bull Extreme Male Enhancement Supplement recalled | Pure Vitamins and Natural Supplements | Undeclared Allergens | NJ |
| Food | CLASS II | Riverence Smoked Trout Dip recalled by Riverence ProvisionsRiverence | Riverence Provisions | Undeclared Milk | 8 states |
| Food | CLASS II | Zarlengo's Chocolate Chip Gelato recalled by Zarlengo Italian IceZarlengo's | Zarlengo Italian Ice | Undeclared Allergens | IL, IN, TX |
| Food | CLASS II | Zarlengo's Double Dark Chocolate Gelato recalled by Zarlengo Italian IceZarlengo's Double | Zarlengo Italian Ice | Undeclared Allergens | IL, IN, TX |
| Food | CLASS II | Crab Cakes various sizes sold to food service recalledCrab | Connecticut Crab Company | Botulism | NJ, NY |
| Food | HEALTH ALERT | Beef and Pork Products recalled by FSIS | FSIS | Undeclared Allergens | |
| Food | HEALTH ALERT | Beef and Pork Products recalled by Sky Ranch Meat | Sky Ranch Meat | Undeclared Sesame | |
| Device | CLASS II | Allura Xper; System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Cardinal Health Monoject Tuberculin Syringe Luer Lock recalled | Cardinal Health 200 | Packaging Defects | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1760, Mmt-1761, Mmt recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Azurion 7 B12 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | 2.4 Volt(tm) Tap Cortex Screw recalled by Synthes (USA) Products | Synthes (USA) Products | Other | Nationwide |
| Device | CLASS II | Allura Xper FD10C recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Anterior Hip Pack Dynj64672b recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1801, Mmt-1805, Mmt-1850, Mmt-1851) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Paradise ¿ Catheter recalled by ReCor Medical | ReCor Medical | Other | Nationwide |
| Device | CLASS II | Vue Motion V12 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Other | Nationwide |
| Device | CLASS II | Azurion 7 M20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper; System recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | BAT (Breast, Axilla and Thyroid) Coverage recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | da Vinci S, Si Tenaculum Forceps Instrument recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Burlington Medical, Kilt recalled | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Allura Xper FD20/20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/15 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS II | Burlington Medical, Caps recalled | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Medline kits containing Olympus biopsy valves: BAL KIT recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Stryker Chromophare Softlit Ring Surgical Light System recalled | Stryker Communications | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Thyroid Shield recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | eTRAX Needle System Starter Kit (for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | Allura Xper/10 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1880, Mmt-1881, Mmt recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | da Vinci S, Si Double Fenestrated Grasper Instrument recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Sterile Radiology Procedure Kits recalled by Medline Industries | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Finesse BTK Multicath Injectable Angioplasty Balloon Catheter recalled | Summa Therapeutics | Other | Nationwide |
| Device | CLASS II | Soltive Pro Laser System Tfl-sls recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits containing Olympus biopsy valves recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Allura Xper FD20/20 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy EV300 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Blue Ventilator Adapter Module, single-patient use circuit recalled | Baxter Healthcare | Other | FL |
| Device | CLASS II | Azurion 5 M20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | eTRAX Needle Sensor -(for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | da Vinci S and Si Monopolar Curved Scissors Instrument recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Artoura Breast Tissue Expanders Reference Numbers recalled | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | Burlington Medical, Blockers recalled | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS I | Trilogy Evo Universal recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo O2 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS II | CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1714, Mmt-1715, Mmt-1754, Mmt-1755) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | RefleXion X1 Radiotherapy System recalled by Reflexion Medical | Reflexion Medical | Device Malfunction | 8 states |
| Device | CLASS II | Azurion 7 M12 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1711, Mmt-1712, Mmt-1751, Mmt-1752) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1884, Mmt-1885, Mmt recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Azurion 3 M15 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Frontal Aprons recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-551, Mmt-751) recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Jiffy Original Composite Polisher Cups (Coarse) recalled | Ultradent Products | Device Malfunction | 31 states |
| Device | CLASS II | Medline kits containing Olympus biopsy valves recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Paradise ¿ Catheter recalled by ReCor Medical | ReCor Medical | Other | Nationwide |
| Device | CLASS II | eTRAX Needle Sensor - (for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | Allura Xper OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Enfit G-tube Connector, Medline recalled by Medline Industries | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | da Vinci S, Si Grasping Retractor Instrument recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Protective Sleeves recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Artoura Breast Tissue Expanders Reference Numbers recalled | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper FD20/10 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | Medline kits containing Olympus biopsy valves: Bronchoscopy recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Kilt Blockers recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Medline Kits containing Enfit G-tube Connector recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Paradigm Real-Time Revel Insulin Pump (Mmt-523, Mmt-723) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | Atellica CH Enzymatic Hemoglobin A1c (A1c_E) recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | Allura Xper FD10F recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Demi Half Aprons recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Soltive Premium Laser System Tfl-pls recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Allura Xper Biplane OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS I | Automated Impella Controller (AIC) recalled by Abiomed | Abiomed | Device Malfunction | MA |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1811, Mmt-1812, Mmt-1861, Mmt-1862) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Burlington Medical, Vest recalled | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Half Aprons recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | eTRAX Needle System Starter Kit (for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | Oxoid Microbact Identification Kits, Listeria Kit, 20 Tests recalled | Oxoid Australia | Listeria | Nationwide |
| Device | CLASS II | Azurion 5 M12 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | eTRAX Needle Sensor -(for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | Paradigm Insulin Pump (Mmt-712, Mmt-715) recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Airway Exam Kit, DYKE1796 recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Azurion 7 B20 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | eTRAX Needle System Starter Kit(for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | Azurion 3 M12 recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | BD Kiestra" ReadA recalled | BD Kiestra LAB Automation | Potency & Assay | 6 states |
| Device | CLASS II | 2.4 Volt Tap Locking Screw Tap recalled by Synthes (USA) Products | Synthes (USA) Products | Other | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump (MMT-1750) recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | CPX 4 US Breast Tissue Expanders recalled by Mentor Texas, LP | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | eTRAX Needle Sensor - (for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | Allura Xper FD20/15 OR Table recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | da Vinci S, Si Mega Needle Driver Instrument recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Leg Wraps recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Paradigm Real-Time Veo Insulin Pump (Mmt-554, Mmt-754) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | Allura Xper Biplane recalled by Philips Medical Systems | Philips Medical Systems Nederl | Device Malfunction | Nationwide |
| Device | CLASS II | Artoura Breast Tissue Expanders Reference Numbers recalled | Mentor Texas | Device Malfunction | Nationwide |
| Device | CLASS II | Wrap Aprons recalled by Burlington Medical | Burlington Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Paradigm Real-Time Insulin Pump (Mmt-522, Mmt-722) recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | eTRAX Needle System Starter Kit (for Aurora Trackers) recalled | Civco Medical Instruments | Processing Deviation | OH, PA, WA |
| Device | CLASS II | MiniMed Insulin Pump (Mmt-1809, Mmt-1810, Mmt recalled | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | da Vinci S, Si Permanent Cautery Hook Instrument recalled | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Signa Premier systems recalled by GE Healthcare | GE Healthcare | Other | Nationwide |
| Device | CLASS II | Thoracic Robots, Dynj908777b recalled by Medline Industries | Medline Industries | Foreign Material | Nationwide |
| Drug | CLASS II | Sterile Eye Drops Soothing Tears recalled by K.C. Pharmaceuticals | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Sterile EYE Drops AC (tetrahydrozoline HCl recalledQuality Choice Eye Drops Irritation Relief | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | EYE Drops Advanced Relief, (dextran recalled by K.C. PharmaceuticalsQuality Choice Moisturizing Relief Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride Capsules, USP, 5mg recalled by Appco PharmaPrazosin Hydrochloride | Appco Pharma | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Sterile Eye Drops Redness Lubricant (glycerin recalledLeader Eye Drops Redness Relief | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Dry Eye Relief Eye Drops, (glycerin recalled by K.C. PharmaceuticalsArtificial Tears | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Sterile Eye Drops Original Formula (tetrahydrozoline HCl 0.05%) recalledGoodsense Eye Drops Original Formula | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Ultra Lubricating Eye Drops (polyethylene recalledLeader Ultra Lubricating Eye Drops | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS II | Artificial Tears Sterile Lubricant Eye Drops recalledLeader Artificial Tears 15 Ml | K.C. Pharmaceuticals | Sterility | Nationwide |
| Drug | CLASS I | Magnesium Sulfate in Water for Injection (40mg/mL) IV recalledMagnesium Sulfate | Amneal Pharmaceuticals | Packaging Defects | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride Capsules, USP, 2mg recalled by Appco PharmaPrazosin Hydrochloride | Appco Pharma | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | traMADol Hydrochloride Tablets, USP, 50 mg recalled | Amneal Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Prazosin Hydrochloride Capsules, USP, 1mg recalled by Appco PharmaPrazosin Hydrochloride | Appco Pharma | Nitrosamine Impurity | Nationwide |
| Food | CLASS III | Mei Heong Yuen Garlic Flavor Roasted Peanuts;; Ingredients recalledMEI Heong | Super World Trading | Other | 19 states |
| Food | CLASS III | Mei Heong Yuen Walnut Flavor Roasted Peanuts;; Ingredients recalledMEI Heong | Super World Trading | Other | 19 states |
| Food | CLASS II | Imu-Tek Colostrum-5 Powder recalled by Imu-Tek Animal HealthImu-Tek Colostrum-5 | Imu-Tek Animal Health, Incorporated | Foreign Material | 30 states |
| Food | CLASS II | Divided Sunset Multi Collagen Peptides, Stand-up recalled by Tg FoodsDivided Sunset | Tg Foods | Undeclared Allergens | 28 states |
| Food | CLASS II | Coconut Drink recalled by Heytea Usa | Heytea Usa | Undeclared Milk | 8 states |
| Food | CLASS III | Mei Heong Yuen Tangerine Flavor Roasted Peanuts recalledMei Heong | Super World Trading | Other | 19 states |
| Food | CLASS II | Imu-Tek Colostrum recalled by Imu-Tek Animal HealthImu-Tek Colostrum-5 | Imu-Tek Animal Health, Incorporated | Foreign Material | 30 states |
| Food | CLASS II | Mama Rose's Prickly Pear Salad Dressing recalled by The Maros GroupMama Rose's | The Maros Group | Undeclared Sulfites | AZ |
| Food | CLASS III | Popping Boba Rtd Peach Oolong Tea recalled by Pocas InternationalPopping Boba | Pocas International | Packaging Defects | 8 states |
| Food | CLASS III | Popping Boba Rtd Mango Passion Fruit Green Tea recalledPopping Boba | Pocas International | Packaging Defects | 8 states |
| Food | CLASS III | Popping Boba Rtd Strawberry Dragon F/oolong Tea recalledPopping Boba | Pocas International | Packaging Defects | 8 states |
| Food | CLASS II | " Dumpling Party Tray Vegetable 011110661173 " Dumpling recalled | JFE Franchising | Foreign Material | 37 states |
| Food | CLASS III | Popping Boba Rtd Mixed Berry Hibiscus Tea recalledPopping Boba | Pocas International | Packaging Defects | 8 states |
| Food | CLASS II | " Dumpling Vegetable 011110658067 " Loaded Dumpling recalled | JFE Franchising | Foreign Material | 37 states |
| Food | CLASS I | Spray Dried Dairy Powder bags or 1 metric ton totes recalled | Lone Star Dairy Products | Salmonella | TX |
| Food | CLASS II | Prickly Pear Jelly recalled by The Maros GroupPrickly Pear | The Maros Group | Undeclared Milk | AZ |
| Food | HEALTH ALERT | FSIS Retracts Public Health Alert for Frozen recalled | | Processing Deviation | |
| Food | HEALTH ALERT | FSIS Retracts Public Health Alert for Frozen recalled by Dorada Foods | Dorada Foods | Lead & Heavy Metals | |
| Device | CLASS I | Trilogy Evo recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS II | Puracol and Puracol Plus Collagen Wound Dressings recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Pelvic Reconstruction System (PRS) recalled by I.T.S | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS III | Philips L12-5 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | HALO PKS Cutting Forceps recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | MicroScan Neg MIC recalled by Beckman Coulter | Beckman Coulter | Other | Nationwide |
| Device | CLASS II | Volar Radius Plate with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS I | Flexible Cryoprobe (OD, L1 recalled by Erbe USA | Erbe USA | Other | Nationwide |
| Device | CLASS III | Philips C9-4 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | BiDop 3 Pocket Doppler (ES-100V3) with BT2M20S8C fetal probe recalled | Koven Technology | Packaging Defects | Nationwide |
| Device | CLASS II | Olympus PKS Cutting Forceps PKS Cutting Forceps recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Everest Bipolar Cutting Forceps recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Pilonplate with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS III | Philips X7-2 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS III | Philips 3D6-2 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | FR.O.H. Calcaneus Repair System recalled by I.T.S | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | Custom Abutment AS Ti, for Straumann RC, incl recalled | Straumann USA | Packaging Defects | Nationwide |
| Device | CLASS II | Embrace Drill Tower, Standard/Lateral recalled | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | 15 states |
| Device | CLASS II | I.T.S. DUL (Distal Ulna Locking) System and UOL recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS III | Philips OMNI III TEE Ultrasound Transducer recalled | Philips Ultrasound | Other | Nationwide |
| Device | CLASS III | Philips Mini Multi TEE Ultrasound Transducer recalled | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | Humeral Head Plate with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS I | DuraMax Chronic Hemodialysis Catheter recalled by Merit Medical Systems | Merit Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Claviculaplate with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | Everest Bipolar Cutting Forceps recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | Tecnis Eyhance Iol with Tecnis Simplicity" Delivery System recalled | AMO Puerto Rico Manufacturing | Device Malfunction | Nationwide |
| Device | CLASS II | I.T.S. Fibula Plate PROlock with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | Custom Abutment Ti, for Straumann RC, incl recalled | Straumann USA | Packaging Defects | Nationwide |
| Device | CLASS II | Olympus Endoscope Air/Water Valve - MAJ recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Handy Solutions Neck & Shoulders Heating Pad, Number recalled | Navajo Manufacturing | Temperature Abuse | Nationwide |
| Device | CLASS I | BioFlo DuraMax Catheter recalled by Merit Medical Systems | Merit Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS III | Philips L17-5 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | I.T.S. LRS (Locking Reconstruction System) recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | Olympus Endoscope Reprocessor OER-Elite recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Tandem pumps are battery-operated infusion pumps capable recalled | Tandem Diabetes Care | Device Malfunction | CA |
| Device | CLASS I | 16F Dual Valved Splittable Sheath Introducer (bulk, non-sterile) recalled | Merit Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Embrace Drill Tower, Wedged recalled by Waldemar Link GmbH & Co. KG | Waldemar Link GmbH & Co. KG (Mfg Site) | Other | 15 states |
| Device | CLASS II | Olympus PK Cutting Forceps PK Cutting Forceps recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS III | Philips OMNI II TEE Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS III | Philips X3-1 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | Olympus Endoscope Reprocessor OER-Pro recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Trilogy Evo O2 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS II | Imactis CT-Navigation System, stereotaxic accessory recalled | GE Medical Systems | Other | Nationwide |
| Device | CLASS III | Philips S4-1 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | PKS Cutting Forceps recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS I | ProGuide Chronic Dialysis Catheters recalled by Merit Medical Systems | Merit Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Endoscope Suction Valve - MAJ recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | Pelvic Reconstruction System (PRS RX & PRS Phoenix) recalled by I.T.S | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | I.T.S. Straight Plate with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS I | Flexible Cryoprobe (OD, L1 recalled by Erbe USA | Erbe USA | Other | Nationwide |
| Device | CLASS I | CentrosFLO Hemodialysis Catheters recalled by Merit Medical Systems | Merit Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Distal Humeral Plates with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | HLS - Hand Locking Plates System recalled by I.T.S | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | Olympus PKS Cutting Forceps PKS Cutting Forceps recalled | Olympus Corporation of the Americas | Device Malfunction | Nationwide |
| Device | CLASS II | I.T.S. Screw System with the below descriptions recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS III | Philips S5-2 Ultrasound Transducer recalled by Philips Ultrasound | Philips Ultrasound | Other | Nationwide |
| Device | CLASS II | Olecranonplate with Angular Stability recalled | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS I | Flexible Cryoprobe (OD, L1 recalled by Erbe USA | Erbe USA | Other | Nationwide |
| Device | CLASS II | FLS - Foot Locking Plates System and HOL recalled by I.T.S | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS I | Trilogy EV300 recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS I | Trilogy Evo Universal recalled by Philips Respironics | Philips Respironics | Device Malfunction | Nationwide |
| Device | CLASS II | HCS - Headless Compression Screw System recalled by I.T.S | I.T.S | Temperature Abuse | Nationwide |
| Device | CLASS II | Drill Plate, Ortho Dev recalled by Orthalign | Orthalign | Potency & Assay | Nationwide |
| Device | CLASS II | Drill Plate, Ortho Dev recalled by Orthalign | Orthalign | Potency & Assay | Nationwide |
| Drug | CLASS II | Curosurf (poractant alfa), 240 mg recalled by Chiesi USACurosurf | Chiesi USA | Sterility | Nationwide |
| Drug | CLASS III | Gelatin Capsule Pack for use recalled by RadnostixSodium Iodide I-131 | Radnostix | Packaging Defects | Nationwide |
| Drug | CLASS II | Meclizine Hydrochloride Tablets, USP 12.5 mg, (a) [] recalledMeclizine Hydrochloride | Amerisource Health Services | Packaging Defects | Nationwide |
| Drug | CLASS II | Octreotide Acetate for Injectable Suspension recalledOctreotide Acetate | Teva Pharmaceuticals USA | Sterility | Nationwide |
| Drug | CLASS II | Octreotide Acetate for Injectable Suspension recalledOctreotide Acetate | Teva Pharmaceuticals USA | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets USP 150 mcg recalled by Macleods Pharma UsaLevothyroxine Sodium | Macleods Pharma USA | Potency & Assay | Nationwide |
| Drug | CLASS II | Octreotide Acetate for Injectable Suspension recalledOctreotide Acetate | Teva Pharmaceuticals USA | Sterility | Nationwide |
| Food | CLASS II | Pepsin 1:10,000 Powder recalled by American LaboratoriesPepsin | American Laboratories | Salmonella | 9 states |
| Food | CLASS II | Bulk packaged Colustrum Powder recalled by Herbal Creations UBulk | Herbal Creations U | Undeclared Milk | CA |
| Food | CLASS II | King Harvest Sundried Tomato Hummus recalled by Pacific Coast FreshKing Harvest | Pacific Coast Fresh | Foreign Material | OR, WA |
| Food | CLASS II | King Harvest Spinach Hummus recalled by Pacific Coast FreshKing Harvest | Pacific Coast Fresh | Foreign Material | OR, WA |
| Food | CLASS I | Espresso Malted Milk Balls sealed pouch recalled by Nuts.comNuts.com | Nuts.com | Undeclared Allergens | Nationwide |
| Food | CLASS I | Doraditas de Azucar recalled by Distribuidora de AlimentosDoraditas | Distribuidora de Alimentos Sendero | Undeclared Allergens | TX |
| Food | CLASS II | Tops GOLD Khatta Meetha Pickle NET QTY recalled by MangalmTops Gold | Mangalm | Other | 5 states |
| Food | CLASS II | Basil Pesto & Mozzarella Pizza recalled by BakkavorBasil Pesto | Bakkavor | Foreign Material | 10 states |
| Food | CLASS II | Pepsin Full Strength Powder recalled by American LaboratoriesPepsin Full | American Laboratories | Salmonella | 9 states |
| Food | CLASS II | Slow Roasted Diced Tomatoes recalled by Sevillo Fine FoodsSlow | Sevillo Fine Foods | Foreign Material | CA, NC |
| Food | CLASS II | Item 6430153 Ajinomoto Vegetable Gyoza Dumplings recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | King Harvest Balsamic Hummus recalled by Pacific Coast FreshKing Harvest | Pacific Coast Fresh | Foreign Material | OR, WA |
| Food | CLASS II | Slow Roasted Diced Tomatoes recalled by Sevillo Fine FoodsSlow | Sevillo Fine Foods | Foreign Material | CA, NC |
| Food | CLASS I | Gorditas de Azucar recalled by Distribuidora de AlimentosGorditas | Distribuidora de Alimentos Sendero | Undeclared Allergens | TX |
| Food | CLASS II | Item 5650893 Ajinomoto Japanese-Style Vegetable Fried Rice made recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Chilli Spanish Peanuts, First Street recalledChilli Spanish | Western Mixers Produce & Nuts | Foreign Material | Nationwide |
| Food | CLASS II | Tops GOLD Mango Pickle NET QTY recalled by MangalmTops Gold | Mangalm | Other | 5 states |
| Food | CLASS II | Item 5650883 Ajinomoto Teppanyaki Style Vegetable Fried Rice recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | King Harvest Jalapeno Hummus recalled by Pacific Coast FreshKing Harvest | Pacific Coast Fresh | Foreign Material | OR, WA |
| Food | CLASS II | Tops GOLD Lime Pickle NET QTY recalled by MangalmTops Gold | Mangalm | Other | 5 states |
| Food | CLASS II | Sunflour Bakery Hamburger Bun containing 6 buns recalledSunflour | NRS Enterprises | Undeclared Sesame | CA |
| Food | CLASS II | Item 5654390 Ajinomoto Golden Tiger Vegetable Fried Rice recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | King Harvest Black Olive Hummus recalled by Pacific Coast FreshKing Harvest | Pacific Coast Fresh | Foreign Material | OR, WA |
| Food | CLASS II | Item 5650173 Trader Joe's Japanese Style Fried Rice with Edamame recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Pan de Bono (Cheese Bread) per Paper Cardboard recalledPan | South Florida Food | Undeclared Soy | FL |
| Food | CLASS II | Item 81153 Kroger Chinese Inspiration Vegetable Fried Rice recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Honey Bbq Sauce Mustard Net recalled by Savannah Bee CompanySavannah Bee | Savannah Bee Company | Undeclared Wheat & Gluten | 45 states |
| Food | CLASS II | Roasted Tomato Parmesan Focaccia Bread sold under the products recalled | Bakkavor | Foreign Material | 10 states |
| Food | CLASS II | King Harvest Roasted Red Pepper Hummus recalled by Pacific Coast FreshKing Harvest | Pacific Coast Fresh | Foreign Material | OR, WA |
| Food | CLASS II | Pepsin 1:3000 Powder recalled by American LaboratoriesPepsin | American Laboratories | Salmonella | 9 states |
| Food | CLASS II | Chilli Spanish Peanuts, Treasured Harvest brand container recalledTreasured Harvest | Western Mixers Produce & Nuts | Foreign Material | Nationwide |
| Food | CLASS II | Lucerne 2% Cottage Cheese 2% Milkfat Small Curd Vitamin recalledLucerne | Albertsons Companies | Foreign Material | 5 states |
| Food | CLASS II | Tops GOLD Mixed Pickle NET QTY recalled by MangalmTops Gold | Mangalm | Other | 5 states |
| Food | CLASS II | Favorina Chocolate Ladybugs German-Style Nougat recalledFavorina | Lidl US TRADING | Other | 10 states |
| Food | CLASS II | Item 5650233 Trader Joe's Vegetable Fried Rice recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Item 81146 Ajinomoto Tai Pei Shrimp Fried Rice - Shrimp recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS I | Mexican Tejocote Roots Supplement Pieces;; Dietary Supplement recalledSiluetaYa | Siluetaya | Other | 6 states |
| Food | CLASS II | Item 6430143 Ajinomoto Vegetable Gyoza Dumplings 12ct recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Tops GOLD Green Chilli Pickle NET QTY recalled by MangalmTops Gold | Mangalm | Other | 5 states |
| Food | CLASS II | 14" Margarita Thin Crust Pizza;. Keep Frozen recalled by Rose and Shore | Rose and Shore | Foreign Material | 5 states |
| Food | CLASS II | Item 81097 Ajinomoto Ling Ling Restaurant Style Fried Rice Savory recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Item 6430093 Ajinomoto Green Gyoza Vegetable & Edamame Dumplings recalledItem | Ajinomoto Foods North America | Foreign Material | 43 states |
| Food | CLASS II | Tops GOLD Stuffed Red Chilli Pickle NET QTY recalled by MangalmTops Gold | Mangalm | Other | 5 states |