| Device | CLASS II | Biomet Ceramic Head Diameter, Type 1, -3 Neck recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | WB XL Anatomic Healing Abutment XC. Endosseous Dental recalled | Straumann USA | Other | Nationwide |
| Device | CLASS II | Tempus Pro Patient Monitor, REFs recalled | Remote Diagnostic Technologies | Device Malfunction | Nationwide |
| Device | CLASS II | NIM Vital Nerve Monitoring System: Console NIM4CM01 NIM recalled | Medtronic Xomed | Device Malfunction | Nationwide |
| Device | CLASS II | Sterile Water Cat T-0780 Sterile Water recalled by Edge Biologicals | Edge Biologicals | Labeling Errors | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | DxI 9000 Access Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | MN |
| Device | CLASS II | Biomet Ceramic Head Diameter, Type 1, +3 Neck recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | BD Pyxis Medbank (Name recalled by CareFusion 303 | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | Rover Mobile X-ray System recalled by Micro-X | Micro-X | Device Malfunction | NJ, PR, WA |
| Device | CLASS II | Rover Mobile X-ray System recalled by Micro-X | Micro-X | Device Malfunction | NJ, PR, WA |
| Device | CLASS II | stryker Latitude EV Humeral Revision Stem Trial, L:, Size recalled | Tornier | Other | MN |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Magec 2 Rod Standard recalled by Globus Medical | Globus Medical | Other | Nationwide |
| Device | CLASS II | Biomet Ceramic Head Diameter, 12/14 Taper, +0 Neck recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Radiometer ABL90 Series - Radiometer ABL90 FLEX recalled | Radiometer Medical ApS | Device Malfunction | 49 states |
| Device | CLASS II | Amplatzer TorqVue LP Catheter (Tvlpc) recalled by Abbott | Abbott | Other | Nationwide |
| Device | CLASS II | Merit Medical recalled | Merit Medical Systems | Other | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Biomet Ceramic Head Diameter, 12/14 Taper, +3 Neck recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recalled | Maquet Cardiovascular | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Brilliance CT Big Bore recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Zenition 50. Product Code 718096. The devices are used recalled | Philips North America | Other | MA |
| Device | CLASS I | Novasight Hybrid System Novasight Hybrid Catheter recalled | Conavi Medical | Packaging Defects | 4 states |
| Device | CLASS II | Biomet Ceramic Head Diameter, Type 1, +0 Neck recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | The Alinity m System is designed to automate the steps recalled | Abbott Molecular | Other | Nationwide |
| Device | CLASS II | Veradius Unity recalled by Philips North America | Philips North America | Other | MA |
| Device | CLASS II | Zenition The device is to be used recalled by Philips Medical Systems | Philips Medical Systems Nederl | Other | Nationwide |
| Device | CLASS II | Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount recalled | IHB Operations | Device Malfunction | Nationwide |
| Device | CLASS II | Zenition 70. Product Code 718133. The devices are used recalled | Philips North America | Other | MA |
| Device | CLASS II | InPen smart insulin pen recalled by Medtronic MiniMed | Medtronic MiniMed | Device Malfunction | 41 states |
| Device | CLASS II | Cell-dyn Ruby recalled by Abbott Laboratories | Abbott Laboratories | Device Malfunction | Nationwide |
| Device | CLASS II | Merit Medical recalled | Merit Medical Systems | Other | Nationwide |
| Device | CLASS II | Amplatzer TorqVue LP Delivery System (TVLP) recalled by Abbott | Abbott | Other | Nationwide |
| Drug | CLASS II | Clindamycin HCl, QTY recalled by RemedyRepack | RemedyRepack | Manufacturing (CGMP) Deviations | PA |
| Drug | CLASS II | Rapidol Arnica Tablets, Homeopathic Medicine recalled by Pharmadel | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | PHENYLephrine HCl in 0.9% Sodium Chloride, 0.5 mg recalled | Denver Solutions | Sterility | Nationwide |
| Drug | CLASS II | Kapsin Ointment, Camphor 3.16% and Capsaicin recalled by Apipharma | Apipharma | Manufacturing (CGMP) Deviations | AZ |
| Drug | CLASS II | Ketamine HCl 50mg per (10 mg per mL) Single Dose Syringe recalled | Denver Solutions | Sterility | Nationwide |
| Drug | CLASS II | Glycopyrrolate, 1mg per, (0.2 mg/mL), Single Dose syringe recalled | Denver Solutions | Sterility | Nationwide |
| Drug | CLASS II | clomiPRAMINE hydrochloride Capsules USP, 25 mg recalledClomipramine Hydrochloride | Lupin Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | dexmedeTOMIDine HCl PF, in 0.9% Sodium Chloride, 20 mcg recalled | Denver Solutions | Sterility | Nationwide |
| Drug | CLASS III | HYDROmorphone Hydrochloride 50mg/ (1mg/mL) recalled by OurPharma | OurPharma | Potency & Assay | Nationwide |
| Drug | CLASS II | DoloEar Earache Drops, Homeopathic fl recalled by Pharmadel | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine recalled | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Kingskin, Elimina Las Verrugas, For the removal of common warts fl recalledKingskin | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Haloperidol Decanoate Injection, 50mg/mL* Single-Dose Vial recalledHaloperidol Decanoate | Amerisource Health Services | Sterility | Nationwide |
| Drug | CLASS II | Haloperidol Decanoate Injection, 100mg/mL*, mL Single-Dose Vials recalledHaloperidol Decanoate | Amerisource Health Services | Sterility | Nationwide |
| Drug | CLASS II | Bimatoprost powder, Bulk Ingredient, a) recalled by Medisca | Medisca | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules USP, 30 mg, a.) bottles recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Haloperidol Decanoate Injection, 100 mg/mL*, mL Single-Dose Vial recalledHaloperidol Decanoate | Amerisource Health Services | Sterility | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules USP, 60 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | DoloDent Maximum Strength Toothache Drops, Homeopathic Oral Drops fl recalled | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Urodel, Urinary Tract Infection Symptoms Relief, Homeopathic recalled | Pharmadel | Manufacturing (CGMP) Deviations | DE |
| Drug | CLASS II | Rocuronium Bromide 50 mg per (10mg per mL) Single Dose Syringe recalled | Denver Solutions | Sterility | Nationwide |
| Drug | CLASS II | Hemopropin Ointment, Lanolin 17.76% and Petrolatum recalled by Apipharma | Apipharma | Manufacturing (CGMP) Deviations | AZ |
| Food | CLASS II | Apple Juice; clear/translucent bulbous/round recalled by S Martinelli & | S Martinelli & | Foreign Material | 28 states |
| Food | CLASS II | Beecher's Street Corn, 8 retail units recalledBeecher's Street | Request Foods Incorporated | Foreign Material | IL, MI |
| Food | CLASS II | Label: Iqf Cilantro Large recalled by Supherb FarmsLabel | Supherb Farms | Foreign Material | 8 states |
| Food | CLASS I | Zaarah Herbals Rasayan Churan recalled by New York Wholesale GroupZaarah Herbals | New York Wholesale Group | Lead & Heavy Metals | 4 states |
| Food | CLASS II | Texas Olive Company Giardiniera All lots recalledTexas Olive | All American Trading Of Houston | Packaging Defects | MS, TX |
| Food | CLASS II | Gold Garlic Powder Irradiated recalled by Pacific Meridian GroupGold Garlic | Pacific Meridian Group | Foreign Material | CA, IL, TX |
| Food | CLASS II | Mexican Street Corn Soup recalled by Request Foods Incorporated | Request Foods Incorporated | Foreign Material | IL, MI |
| Food | CLASS II | Moroccan Style Lentil Soup recalled by Request Foods IncorporatedMoroccan | Request Foods Incorporated | Foreign Material | IL, MI |
| Food | CLASS II | Cuban-Style Black Bean Soup recalled by Request Foods IncorporatedCuban-Style | Request Foods Incorporated | Foreign Material | IL, MI |
| Food | CLASS II | Magic Flame, Hulled Sunflower Kernels, Bakery Grade, 501b recalledMagic Flame | JJ Nuts | Foreign Material | MD, PA |
| Food | CLASS I | Zaarah Herbals Vasaka Powder recalled by New York Wholesale GroupZaarah Herbals | New York Wholesale Group | Lead & Heavy Metals | 4 states |
| Food | CLASS II | Texas Olive Company Capers Capote recalled by All American Trading OfTexas Olive | All American Trading Of Houston | Packaging Defects | MS, TX |
| Food | CLASS II | Label: Frozen Chopped Cilantro recalled by Supherb FarmsLabel | Supherb Farms | Foreign Material | 8 states |
| Food | CLASS I | Cfs Cromer Food Services, Inc. Anderson recalledCFS Cromer | Cromer Food Services | Undeclared Milk | GA, SC |
| Food | CLASS I | Zaarah Herbals Gurmar Powder recalled by New York Wholesale GroupZaarah Herbals | New York Wholesale Group | Lead & Heavy Metals | 4 states |
| Food | CLASS I | Mo-cha Premium Non-Dairy Creamer recalled by Momo TeaMo-cha | Momo Tea | Undeclared Allergens | CT, NJ, NY |
| Food | CLASS I | Zaarah Herbals Bhringraj Powder recalled by New York Wholesale GroupZaarah Herbals | New York Wholesale Group | Lead & Heavy Metals | 4 states |
| Food | CLASS I | Walker's Wine Juice Pumpkin Juice 2.5, 5, 30, 60 bulk containers recalledWalker's | Walker's Fruit Basket and Press House | Botulism | 12 states |
| Food | CLASS II | Texas Olive Co. Pepperoncini glass recalled by All American Trading OfTexas Olive | All American Trading Of Houston | Packaging Defects | MS, TX |
| Food | CLASS I | Spermidine, Maximum Strength, 10 mg per serving recalledSpermidine | Supplement Manufacturing Partner | Undeclared Allergens | Nationwide |
| Food | CLASS I | Sausage and Sliced Meat and Poultry Products recalled by Smith Packing | Smith Packing | Processing Deviation | |
| Food | CLASS I | Pork Bun Products recalled by ACC Central Kitchen | ACC Central Kitchen | Undeclared Sesame | |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Precip Tray recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Pain Pack recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Basic Cataract recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Aveir DR Leadless Pacemaker (LP) Ventricular Device recalled | Abbott Medical | Temperature Abuse | Nationwide |
| Device | CLASS II | Refer to RES recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Venue Fit recalled by GE Medical Systems | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS I | Tandem Mobi Insulin Pump with Interoperable Technology recalled | Tandem Diabetes Care | Labeling Errors | 29 states |
| Device | CLASS II | Cerene Cryotherapy Device, Thermal Ablation, Endometrial recalled | Channel Medsystems | Packaging Defects | Nationwide |
| Device | CLASS II | Id Now Covid-19 2.0 24t recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Device Malfunction | Nationwide |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Welch Allyn Connex Integrated Wall System recalled by Baxter Healthcare | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS II | Philips DXR System, DuraDiagnost recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Maquet VH-3010 Power Supply recalled by Maquet Cardiovascular | Maquet Cardiovascular | Other | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Peri Gyn Pack recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Guide Wire with Ruler Tube mm DIA recalled by Stryker | Stryker | Foreign Material | Nationwide |
| Device | CLASS II | TLX/TLC SP Guided Implant Driver, for ratchet, stainless steel recalled | Straumann USA | Foreign Material | Nationwide |
| Device | CLASS II | Welch Allyn Green Series 777 Wall System recalled by Baxter Healthcare | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS II | Refer to RES recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Id Now Rsv 24t recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Potency & Assay | Nationwide |
| Device | CLASS II | Welch Allyn CP150 Electrocardiograph recalled by Baxter Healthcare | Baxter Healthcare | Hidden Drug Ingredients | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Guide Wire with Ruler Tube mm DIA recalled by Stryker | Stryker | Foreign Material | Nationwide |
| Device | CLASS II | Rover Mobile X-ray System recalled by Micro-X | Micro-X | Device Malfunction | Nationwide |
| Device | CLASS II | Rover Mobile X-ray System recalled by Micro-X | Micro-X | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: IV Pack South recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | BD Single-Lumen PowerPICC Catheters recalled by Bard Access Systems | Bard Access Systems | Packaging Defects | Nationwide |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: T A PACK recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | HeartMate Mobile Power Unit recalled by Thoratec | Thoratec | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Philips DXR System, DuraDiagnost Rel recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS I | AutoPulse NXT Resuscitation System AutoPulse NXT Platform recalled | Zoll Circulation | Device Malfunction | 18 states |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | restor3d Cordera Hip System recalled by Conformis | Conformis | Labeling Errors | Nationwide |
| Device | CLASS II | Id Now Covid-19 2.0 24t recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Standard D&C recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Welch Allyn Spot Vital Signs 4400 Device recalled by Baxter Healthcare | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS II | Medflex, REF: 1119-00; Medbank Main, REF: 1137-00; Medflex 2.0, REF recalled | CareFusion 303 | Device Malfunction | Nationwide |
| Device | CLASS II | ID NOW Influenza A/B 2 24T recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Potency & Assay | Nationwide |
| Device | CLASS II | Welch Allyn 2-Piece Reusable Blood Pressure Cuff Kits recalled | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Dental Pack-lf recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Welch Allyn DuraShock Aneroid Gauge Sets recalled by Baxter Healthcare | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS II | Welch Allyn Connex Accessory Power Management Stand recalled | Baxter Healthcare | Hidden Drug Ingredients | Nationwide |
| Device | CLASS II | Welch Allyn Welch Allyn Connex Spot Monitor recalled | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS II | Id Now Rsv 24t recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Potency & Assay | Nationwide |
| Device | CLASS II | Welch Allyn Connex Vital Signs Monitor recalled by Baxter Healthcare | Baxter Healthcare | Labeling Errors | IL |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: T&a Endo Pack recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: CW PERI GYN recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Refer to RES recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Welch Allyn Connex Vital Signs Monitor (CVSM) recalled | Baxter Healthcare | Hidden Drug Ingredients | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS I | t:slim X2 Insulin Pump with Interoperable Technology recalled | Tandem Diabetes Care | Labeling Errors | 29 states |
| Device | CLASS I | Ballard Closed Suction Catheters recalled by Avanos Medical | Avanos Medical | Sterility | Nationwide |
| Device | CLASS II | ID NOW Influenza A/B 2 24T recalled by Abbott Diagnostics Scarborough | Abbott Diagnostics Scarborough | Potency & Assay | Nationwide |
| Device | CLASS II | Medline Convenience kits used for various procedures: Nail Pack recalled | Medline Industries LP - Northfield | Sterility | Nationwide |
| Drug | CLASS II | ChlorproMAZINE Hydrochloride Tablets, USP, 10 mg recalled | The Harvard Drug Group | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Unisom, SleepMinis, Diphenhydramine HCl, Mini-Capsules recalled | Chattem | Nitrosamine Impurity | Nationwide |
| Drug | CLASS I | Levetiracetam 0.75% in Sodium Chloride Injection 1,000 mg recalledLevetiracetam | Dr. Reddy's Laboratories | Labeling Errors | Nationwide |
| Drug | CLASS II | Testosterone Cypionate Injection, USP, CIII, 200mg per mL recalledTestosterone Cypionate | Eugia US | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Ciprofloxacin Ophth Solution recalled by Direct Rx | Direct Rx | Packaging Defects | 5 states |
| Food | CLASS II | Falafel King Taste the Mediterranean is a multi-component recalledFalafel King | Falafel King Enterprises | Undeclared Sesame | CO |
| Food | CLASS III | BaiWei ShanZhuang, Dried Seedless Plum Candy recalledBaiWei ShanZhuang | Tristar Food Wholesale Co | Foreign Material | 11 states |
| Food | CLASS II | Tortilla Chip Green 4 cut packed recalledTortilla Chip | La Mexicana Tortilla Factory | Undeclared Allergens | TX |
| Food | CLASS III | Farmer House Preserve Olive Strips recalled by Lins Waha InternationalFarmer House | Lins Waha International | Other | 18 states |
| Food | CLASS II | Dark Chocolate Almond Sea Salt recalled by Tony's ChocolonelyTony's Chocolonely | Tony's Chocolonely | Foreign Material | Nationwide |
| Food | CLASS I | Marketside celery stick recalled by Duda Farm Fresh FoodsMarketside | Duda Farm Fresh Foods | Listeria | Nationwide |
| Food | CLASS II | Arepas de Chocolo, Abuelas Food Company, Delicias de la Abuela's recalledArepas | Delicias De La Abuela | Undeclared Allergens | FL |
| Food | CLASS II | Everything Bar recalled by Tony's ChocolonelyTony's Chocolonely | Tony's Chocolonely | Foreign Material | Nationwide |
| Food | CLASS II | Rolled Oats recalled by Grain MillersRolled | Grain Millers | Foreign Material | CA, IN |
| Food | CLASS I | Trader Joe's Hot Honey Mustard Dressing recalled by Reser's Fine FoodsTrader Joe's | Reser's Fine Foods | Undeclared Peanuts | 18 states |
| Food | CLASS II | Panaderia/Bakery Salvadorena recalled by Panaderia Salvadorena IiPanaderia | Panaderia Salvadorena Ii | Undeclared Milk | MA, RI |
| Food | CLASS II | Golden Crop Candy un-wrapped candies) recalled by Blooming Import | Blooming Import | Undeclared Allergens | 8 states |
| Food | CLASS II | Golden Crop Candy wrapped candies) recalled by Blooming Import | Blooming Import | Undeclared Allergens | 8 states |
| Food | CLASS III | Lemon Plum recalled by Rong Shing Trading NY | Rong Shing Trading NY | Undeclared Sulfites | 5 states |
| Food | CLASS II | Legally Addictive The O.g. Cookies Made recalledLegally Addictive | Legally Addictive Foods | Other | IL, PA |
| Food | HEALTH ALERT | Pork Carnitas Products recalled by Cargill Meat Solutions | Cargill Meat Solutions | Foreign Material | |
| Device | CLASS II | stryker Blueprint Mixed Reality Glenoid Box Lid recalled | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS I | Medline medical convenience kits labeled as recalled | Medline Industries LP - Northfield | Other | CA |
| Device | CLASS II | GenetiSure Dx Labeling Kit recalled by Agilent Technologies | Agilent Technologies | Potency & Assay | MA |
| Device | CLASS I | Medline medical procedure kits recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Other | 9 states |
| Device | CLASS II | Wayson Hydrocolloid recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Medline ReNewal ENT Coblator II PROcise mAx,W/ Integrated recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS I | Medline medical procedure kits recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Other | 9 states |
| Device | CLASS II | stryker HoloBlueprint Application recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS I | Medline medical procedure kits recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Other | 9 states |
| Device | CLASS II | stryker Blueprint Mixed Reality Instrument Check Block recalled | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality BP MxR Glenoid Pin Guide recalled | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS I | Hippo 072 Aspiration System including Cheetah Delivery Tool recalled | Qapel Medical | Device Malfunction | 29 states |
| Device | CLASS II | BD Pyxis MedBank Cubie Replenishment Station Product recalled | CareFusion 303 | Device Malfunction | 32 states |
| Device | CLASS II | DxI 9000 Access Immunoassay Analyzer recalled by Beckman Coulter | Beckman Coulter | Potency & Assay | MN |
| Device | CLASS II | Atellica CH Revised C Reactive Protein (RCRP) recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | Medline ReNewal Coblator II Evac 70 Xtra Plasma recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | FilmArra Pneumonia Panel plus (Pneumoplus) recalled | BioFire Diagnostics | Device Malfunction | UT |
| Device | CLASS II | Wayson Hydrocolloid recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Sterility | Nationwide |
| Device | CLASS II | Stimulation RC Clinician Programmer Application recalled | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS II | IVX Station Reconstitution Transfer Set recalled by Omnicell | Omnicell | Sterility | AL |
| Device | CLASS I | Medline medical procedure kits recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Other | 9 states |
| Device | CLASS II | Medline ReNewal Coblator II ENT Evac 70 Xtra recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | stryker Blueprint Mixed Reality Box Base recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | Medline ReNewal ENT Coblator II PROcise XP recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | stryker Blueprint Mixed Reality Instrument Kit recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality Depth Stop Pin recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality Glenoid Digitizer recalled | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | stryker Blueprint Mixed Reality Coracoid Clamp recalled by Tornier S.A.S | Tornier S.A.S | Device Malfunction | 7 states |
| Device | CLASS II | BD Pyxis" MedBank" Mini and BD Pyxis" MedBank" Tower recalled | CareFusion 303 | Device Malfunction | Nationwide |
| Drug | CLASS II | Fluphenazine Hydrochloride Tablets 2.5mg recalledFluphenazine Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Teriflunomide Tablets, 14mg recalled by Glenmark PharmaceuticalsTeriflunomide | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Solifenacin Succinate Tablets 10MG, a. bottle recalledSolifenacin Succinate | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Voriconazole Tablets 200 mg recalled by Glenmark PharmaceuticalsVoriconazole | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Propafenone Hydrochloride Extended-Release Capsules 225mg recalledPropafenone Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Proactiv Emergency Blemish Relief (Benzoyl Peroxide 5%) recalled | Alchemee | Benzene | Nationwide |
| Drug | CLASS II | Lacosamide Tablets, 50mg recalled by Glenmark PharmaceuticalsLacosamide | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Haloperidol Decanoate Injection 100mg/mL Single-Dose Vial recalledHaloperidol Decanoate | Somerset Therapeutics Private | Sterility | Nationwide |
| Drug | CLASS II | Nitroglycerin Sublingual Tablets 0.3MG recalledNitroglycerin | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Gabapentin Capsules, USP 300 mg recalledGabapentin | SUN Pharmaceutical Industries | Packaging Defects | Nationwide |
| Drug | CLASS II | Clindamycin Hydrochloride Capsules, USP, 300mg recalledClindamycin Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Indomethacin Extended-Release Capsules, 75mg recalledIndomethacin | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Rosuvastatin Tablets 40mg recalled by Glenmark PharmaceuticalsRosuvastatin Calcium | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Propafenone Hydrochloride Extended-Release Capsules, USP 325mg recalledPropafenone Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Fluphenazine Hydrochloride Tablets, 10mg recalledFluphenazine Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Lacosamide Tablets 200mg recalled by Glenmark PharmaceuticalsLacosamide | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Haloperidol Decanoate Injection 50mg/mL Single-Dose Vial recalledHaloperidol Decanoate | Somerset Therapeutics Private | Sterility | Nationwide |
| Drug | CLASS II | 0.9% Sodium chloride Irrigation USP, Isotonic Solution recalledSodium Chloride | B. Braun Medical | Particulate Matter | Nationwide |
| Drug | CLASS II | Diltiazem Hydrochloride Extended-Release Capsules 12HR recalledDiltiazem Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Pravastatin Sodium Tablets 80mg recalled by Glenmark PharmaceuticalsPravastatin Sodium | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Rufinamide Tablets 200mg recalled by Glenmark PharmaceuticalsRufinamide | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Haloperidol Decanoate Injection, 100 mg/mL Single-Dose Vial recalledHaloperidol Decanoate | Somerset Therapeutics Private | Sterility | Nationwide |
| Drug | CLASS II | Propafenone Hydrochloride Extended-Release Capsules USP, 225mg recalledPropafenone Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Proactiv Skin Smoothing Exfoliator (Benzoyl Peroxide 2.5%) recalled | Alchemee | Benzene | Nationwide |
| Drug | CLASS II | Carvedilol Tablets, USP 12.5 mg recalled by Glenmark PharmaceuticalsCarvedilol | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Pravastatin Sodium Tablets, USP, 20mg, a) recalledPravastatin Sodium | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Methocarbamol Injection USP 1,000 mg/ (100 mg/mL) Single Dose Vial recalledMethocarbamol | Somerset Therapeutics Private | Sterility | Nationwide |
| Drug | CLASS II | Lacosamide Tablets, 100mg recalled by Glenmark PharmaceuticalsLacosamide | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Acetaminophen and Ibuprofen (Nsaid) Tablets, 250 mg/125 mg a) recalledAcetaminophen, Ibuprofen | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Nitroglycerin Sublingual Tablets 0.4MG recalledNitroglycerin | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Saxagliptin Tablets 5mg, a) recalled by Glenmark PharmaceuticalsSaxagliptin | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Colesvelam Hydrocholoride Tablets 625mg recalledColesevelam Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Voriconazole Tablets 50mg recalled by Glenmark PharmaceuticalsVoriconazole | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Propafenone Hydrochloride Extended-Release Capsules 325mg recalledPropafenone Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Lacosamide Tablets 150mg recalled by Glenmark PharmaceuticalsLacosamide | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Saxagliptin Tablets, USP, 2.5mg, a) recalled by Glenmark PharmaceuticalsSaxagliptin | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Prochlorperazine Maleate Tablets, 10mg recalled | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Venlafaxine Tablets, USP, 75 mg recalled by Zydus Pharmaceuticals (USA)Venlafaxine | Zydus Pharmaceuticals | Foreign Material | Nationwide |
| Drug | CLASS III | Gabapentin Capsules, USP 400 mg recalledGabapentin | SUN Pharmaceutical Industries | Packaging Defects | Nationwide |
| Drug | CLASS II | Gabapentin Tablets 600mg recalled by Glenmark PharmaceuticalsGabapentin | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Solifenacin Succinate Tablets 5mg, a.) bottle recalledSolifenacin Succinate | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | chlorproMAZINE Hydrochloride Tablets, USP 10 mg recalledChlorpromazine Hydrochloride | Zydus Pharmaceuticals | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Metformin Hydrochloride Extended-Release Tablets 1000mg recalledMetformin Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Pravastatin Sodium Tablets, 20mg, a) recalledPravastatin Sodium | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Naproxen Sodium Tablets, USP, 550mg recalled by Glenmark PharmaceuticalsNaproxen Sodium | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Frovatriptan Succinate Tablets 2.5mg recalledFrovatriptan Succinate | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Fenofibrate Capsules 67 mg recalled by Glenmark PharmaceuticalsFenofibrate | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Pravastatin Sodium Tablets, USP, 80mg, a) recalledPravastatin Sodium | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Ranolazine Extended-Release Tablets 1000mg recalledRanolazine | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Sofosbuvir and Velpatasvir, 400 mg/: blister cards recalledSofosbuvir And Velpatasvir | Asegua Therapeutics | Packaging Defects | Nationwide |
| Drug | CLASS II | Cetirizine Hydrochloride Tablets, USP, 10mg packs recalledCetirizine Hcl | Glenmark Pharmaceuticals Inc., USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Haloperidol Decanoate Injection 50mg/mL Single-Dose Vial recalledHaloperidol Decanoate | Somerset Therapeutics Private | Sterility | Nationwide |
| Food | CLASS II | Lillie's Q Buffalo Wing Sauce recalled by Old World Spices & SeasoningLillie's Q | Old World Spices & Seasoning | Undeclared Milk | 13 states |
| Food | CLASS II | Teriyaki Sauce, Red Shell branded recalledTeriyaki | Red Shell Foods | Other | CA |
| Food | CLASS I | Las Ollas Botana Mix snack recalled by KedakeLas Ollas | Kedake | Undeclared Sesame | TX |
| Food | CLASS II | Multi-v Men's Daily Multivitamin dietary supplement recalled by Mtn OpsMtn Ops | Mtn Ops | Undeclared Soy | Nationwide |
| Food | CLASS II | Dried Cranberries/case recalled by Victor Packing | Victor Packing | Labeling Errors | 9 states |
| Food | CLASS II | Dr. Praeger s California Veggie Fries recalledDr. Praeger | Dr. Praeger's Sensible Foods | Undeclared Allergens | 15 states |
| Food | CLASS I | 365 Whole Foods Market Small Bites Macaroni & Cheese recalled | C.H. Guenther & Son | Undeclared Allergens | Nationwide |
| Food | CLASS II | Desert Farms Jalapeno Mustard recalled by The Truck FarmDesert | The Truck Farm | Foreign Material | Nationwide |
| Food | CLASS III | Cabot Creamery Extra Creamy Premium Butter, Sea Salted recalledCabot | Agri-mark | Packaging Defects | 7 states |
| Food | CLASS II | Brioche Bread Loaf and Hamburger buns recalledBrioche | Harvey Investments LLC / The Baking Group | Undeclared Allergens | TX |
| Food | HEALTH ALERT | Various Soup & Bowl Products recalled by FSIS | FSIS | Foreign Material | |
| Device | CLASS II | Cordis, REF: C09060ML, Smart Control Vascular Stent System recalled | Cordis US | Packaging Defects | 5 states |
| Device | CLASS I | ID Circuit Flex recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS II | Pdsii¿vio¿¿usp6-0(m0.7)¿d/a¿c recalled by Ethicon Endo Surgery | Ethicon Endo Surgery | Other | Nationwide |
| Device | CLASS II | DxC 500 AU Clinical Chemistry Analyzer recalled by Beckman Coulter | Beckman Coulter | Device Malfunction | Nationwide |
| Device | CLASS II | Nasopore Standard fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Ethibond Excel Grn Usp2-0(m3) D/a Mh recalled by Ethicon Endo Surgery | Ethicon Endo Surgery | Other | Nationwide |
| Device | CLASS II | Monterey AL Implant Inserter recalled by Stryker Spine | Stryker Spine | Other | 13 states |
| Device | CLASS I | Anesthesia Circuit Kit Flex (P)2 recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kit Flex recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kit Flex recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS II | Monterey AL Implant Inserter recalled by Stryker Spine | Stryker Spine | Other | 13 states |
| Device | CLASS II | Otopore Cylinder Standard outer ear dressings recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | A820 myPTM recalled by Medtronic Neuromodulation | Medtronic Neuromodulation | Device Malfunction | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kit Flex EPA recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS II | BD Connecta BD Luer-Lok recalled by Bd Switzerland Sarl | BD Switzerland Sarl | Other | 35 states |
| Device | CLASS II | QIAstat-Dx Respiratory Panel Plus Reference Number recalled | Qiagen Sciences | Device Malfunction | 12 states |
| Device | CLASS II | Terumo CDI OneView Monitoring System Hematocrit / Oxygen recalled | Terumo Cardiovascular Systems | Device Malfunction | 6 states |
| Device | CLASS II | Pacific Hemostasis Thromboplastin-D Used recalled by Fisher Diagnostics | Fisher Diagnostics | Potency & Assay | PA |
| Device | CLASS II | Monterey AL Implant Inserter recalled by Stryker Spine | Stryker Spine | Other | 13 states |
| Device | CLASS II | Nasopore fragmentable nasal dressing, Firm recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Nasopore Ex Firm fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Centricity Pacs-iw (Pacs-iw) recalled by GE Healthcare | GE Healthcare | Other | IL |
| Device | CLASS II | Nasopore Ex Firm fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Boppli: Bedside Device Kit recalled by Pyrames | Pyrames | Device Malfunction | CA, MA |
| Device | CLASS II | Phoroptor VRx Digital Refraction System recalled by Reichert | Reichert | Other | Nationwide |
| Device | CLASS II | Nasopore Standard fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Nasopore fragmentable nasal dressing, Firm recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Nasopore Standard fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS I | Anesthesia Circuit Kit Flex recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS II | Prolene Blu Usp6-0(m0.7) S/a P-1 Prm recalled by Ethicon Endo Surgery | Ethicon Endo Surgery | Other | Nationwide |
| Device | CLASS II | Pds¿plus¿vio¿¿usp6-0(m0.7)¿d/a¿c-1¿mp recalled | Ethicon Endo Surgery | Other | Nationwide |
| Device | CLASS II | Cordis, REF C10040ML, Smart Control Vascular Stent System recalled | Cordis US | Packaging Defects | 5 states |
| Device | CLASS II | Nasopore Standard fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Phoroptor VRx Digital Refraction System recalled by Reichert | Reichert | Other | Nationwide |
| Device | CLASS II | Hemopore nasal/sinus temporary wound dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS I | VentStar Flex recalled by Draeger | Draeger | Device Malfunction | Nationwide |
| Device | CLASS II | Centricity Pacs-iw with Universal Viewer recalled by GE Healthcare | GE Healthcare | Other | IL |
| Device | CLASS II | Monterey AL Implant Inserter recalled by Stryker Spine | Stryker Spine | Other | 13 states |
| Device | CLASS II | Hemopore nasal/sinus temporary wound dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Otopore Square outer ear wound dressing, Firm recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Pacific Hemostasis Thromboplastin-D Used recalled by Fisher Diagnostics | Fisher Diagnostics | Potency & Assay | PA |
| Device | CLASS II | Nasopore FD fragmentable nasal dressing recalled by Stryker | Stryker | Sterility | Nationwide |
| Device | CLASS II | Otopore Cylinder outer ear wound dressing, Firm recalled by Stryker | Stryker | Sterility | Nationwide |
| Drug | CLASS II | chlorproMAZINE Hydrochloride Tablets, USP 100 mg recalledChlorpromazine Hydrochloride | Glenmark Pharmaceuticals Inc., USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Duloxetine Delayed-Release Capsules, USP, 30 mg recalledDuloxetine | Breckenridge Pharmaceutical | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Voriconazole Tablets, 50 mg recalled by Amerisource Health ServicesVoriconazole | Amerisource Health Services | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS III | Tropicamide - Proparacaine - Phenylephrine recalled by Imprimis NJOF | Imprimis Njof | Potency & Assay | FL, NY |
| Drug | CLASS III | Tolterodine Tartrate Extended-Release Capsules, 2 mg Dose recalled | The Harvard Drug Group | Potency & Assay | Nationwide |
| Drug | CLASS II | Atorvastatin Calcium Tablets USP 40 mg recalled by Biocon PharmaAtorvastatin Calcium | Biocon Pharma | Potency & Assay | Nationwide |
| Food | CLASS II | Good & Gather baby Pea, Zucchini, Kale & Thyme Vegetable Puree recalledGood | Fruselva U | Lead & Heavy Metals | Nationwide |
| Food | CLASS II | Lean Cuisine Butternut Squash Ravioli recalledLean Cuisine | Nestle-USA, Inc. (Corporate Office) | Foreign Material | 37 states |
| Food | CLASS II | De Nata; Ingredients: Flour, Vegetable Oil, Sugar recalledJulie's Gorditas | Julie's Gorditas | Undeclared Allergens | CA |
| Food | CLASS II | Smokedhouse Alehouse Clam Chowder recalled by SeabearSeaBear Smokedhouse | Seabear | Botulism | Nationwide |
| Food | CLASS II | Kashk (Whey) Ingredients: Whey, Water recalled by Nader TradingKashk | Nader Trading | Undeclared Allergens | CA, MD, VA |
| Food | CLASS II | Panang Curry Tofu Vegan GF is a refrigerated recalledPanang Curry | Seattle Homemade Thai | Undeclared Soy | WA |
| Food | CLASS II | US Foods Premium Monster Cookie recalled by Craftmark Bakery | Craftmark Bakery | Foreign Material | CA, IL, MD |
| Food | CLASS I | Choshiya branded "Aokappa Zuke Prepared Mix Vegetables" recalledChoshiya | AKT Trading | Packaging Defects | CA |
| Food | CLASS I | Choshiya branded "Fukushin Zuke Prepared Mix Vegetables" recalledChoshiya | AKT Trading | Packaging Defects | CA |
| Food | CLASS II | Fresh Flax Oil Omega 3-6-9 Organic Flaxseed Oil recalled | Bioriginal Food & Science | Undeclared Allergens | PR |
| Food | CLASS I | Tostitos Cantina Traditional Yellow Corn Tortilla Chips recalledTostitos Cantina | Frito-Lay, Inc. Headquarters | Undeclared Allergens | 13 states |
| Food | CLASS II | Lean Cuisine Spinach Artichoke Ravioli recalledLean Cuisine | Nestle-USA, Inc. (Corporate Office) | Foreign Material | 37 states |
| Food | CLASS II | Smokedhouse Salmon Chowder recalled by SeabearSeaBear Smokedhouse | Seabear | Botulism | Nationwide |
| Food | CLASS I | Choshiya branded "Menma Ajitsuke Prepared Bamboo Shoots" recalledChoshiya | AKT Trading | Packaging Defects | CA |
| Food | CLASS II | Lean Cuisine Lemon Garlic Shrimp Stir Fry recalledLean Cuisine | Nestle-USA, Inc. (Corporate Office) | Foreign Material | 37 states |
| Food | CLASS II | Cacao Barry Gianduja Noir plastic bucket, 8 buckets recalledCacao Barry | Barry Callebaut USA | Undeclared Milk | 8 states |
| Food | CLASS I | Choshiya branded "Soft Tsubozuke Prepared Mix Vegetables" recalledChoshiya | AKT Trading | Packaging Defects | CA |
| Food | CLASS I | Choshiya branded "Shiba Zuke Prepared Mix Vegetables" recalledChoshiya | AKT Trading | Packaging Defects | CA |
| Food | CLASS II | Turkey BLT on Sourdough recalled by The Coastal Companies | The Coastal Companies | Undeclared Allergens | NY |
| Food | CLASS II | 5000642 CraftMark Oatmeal Cranberry Raisin Cookie Dough recalled | Craftmark Bakery | Foreign Material | CA, IL, MD |
| Food | CLASS I | Choshiya branded "Rakkyo Zuke Prepared Vegetables" recalledChoshiya | AKT Trading | Packaging Defects | CA |
| Food | CLASS II | 5000108 Oatmeal Raisin Cookie Dough, 6 of 30 frozen pucks recalled | Craftmark Bakery | Foreign Material | CA, IL, MD |
| Food | CLASS I | Cheddar Bratwurst Product recalled by Momence Real Estate | Momence Real Estate | Foreign Material | |
| Device | CLASS II | Baxter Mobile column TruSystem recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter Floor mounting column TS recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter Floor mounting column TruSystem recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Angio Drape Pack recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS I | CVAC Aspiration System recalled by Calyxo | Calyxo | Other | Nationwide |
| Device | CLASS II | NexGen LPS Flex, Knee joint patellofemorotibial recalled by Zimmer | Zimmer | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter TruSystem 7500 Hybrid Plus (SC) recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Breast Pack-lf, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Baxter TruSystem 7500 Hybrid (FC) recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Banner Health Systems Lap Pack recalled by American Contract Systems | American Contract Systems | Sterility | AZ |
| Device | CLASS II | Medline procedure kits labeled as: C Section, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: L S GYN PACK, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Progressa Bed Surfaces, intended to be used to treat recalled | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Angio Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Baxter Operating table column TS7500 Mobius recalled | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | namic convenience kits labeled as: KIT,Arterial,60,PG recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: CT Biopsy Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Baxter TruSystem 7500 Hybrid MR Imris recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Acl Arthroscopy Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: A & A Knee Pack-lf, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: General Endoscopy Pack recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Baxter Stationary column TruSystem recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Checkpoint Guardian Intraoperative Lead, Medium recalled | Checkpoint Surgical | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Aop/Basic Eye Pack-lf recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | (Stenfilcon A) Contact Lens recalled by CooperVision | CooperVision | Mold | 15 states |
| Device | CLASS II | Baxter NovumIQ Syringe Infusion System recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Medline ReNewal Reprocessed Livewire Steerable recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | Checkpoint Guardian Intraoperative Lead, Small recalled | Checkpoint Surgical | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Arthroscopy Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Premier Solo Diamond - Large Invented Cone recalled | Premier Dental Products | Other | Nationwide |
| Device | CLASS I | Shiley Adult Flexible Tracheostomy Tube recalled by Covidien | Covidien | Device Malfunction | CO |
| Device | CLASS II | Medline procedure kits labeled as: Delivery Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Helix Elite Inactivated Standard recalled by Microbiologics | Microbiologics | Potency & Assay | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Clovis Robotic-lf, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | namic convenience kits labeled as recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | namic convenience kits labeled as: Pml,72,Adult,Fll-mll,-,Oem recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: AV Fistula Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Banner Health Systems Cysto Pack recalled by American Contract Systems | American Contract Systems | Sterility | AZ |
| Device | CLASS II | Medline procedure kits labeled as: Bilateral Facet Tray, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: CV Neonatal Pack recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as recalled by MEDLINE INDUSTRIES, LP | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Ablation Pack, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Baxter TruSystem 7500 Hybrid (SC) recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter TruSystem 7500 Hybrid (MC) recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Prelude Ideal 4 F Hydrophilic Sheath Introducer recalled | Merit Medical Systems | Other | UT |
| Device | CLASS II | Medline procedure kits labeled as: Acoustic Neuroma Pack-lf recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Baxter Stationary column TruSystem recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter TruSystem recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | CardioMEMS Heart Failure (HF) System that consist recalled | St. Jude Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Orthofix Pillar SA Ti Spacer System Intervertebral Body recalled | Orthofix U.S | Labeling Errors | Nationwide |
| Device | CLASS II | Baxter Mobile column TruSystem recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | Baxter TruSystem 7500 Hybrid Plus (FC) recalled by Baxter Healthcare | Baxter Healthcare | Device Malfunction | Nationwide |
| Device | CLASS II | namic convenience kits labeled as: Mts,4 Valve,Lft,Hrt,Kit-ahs-a*,NW recalled | Medline Industries LP - Northfield | Other | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Laceration Tray recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: Angiography Specials recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Medline procedure kits labeled as: AV Fistula Pack-lf, Pack Number recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Device | CLASS II | Banner University Med Ctr Cardiac Cath Lab Pack recalled | American Contract Systems | Sterility | AZ |
| Device | CLASS II | Medline procedure kits labeled as: C Scope Disposable Kit recalled | Medline Industries LP - Northfield | Foreign Material | Nationwide |
| Drug | CLASS II | Testosterone Gel 1%-dose packets recalled by Strides PharmaTestosterone | Strides Pharma | Benzene | Nationwide |
| Drug | CLASS II | fentaNYL Citrate PF 200 mcg recalled by QuVa Pharma | QuVa Pharma | Sterility | Nationwide |
| Drug | CLASS II | babyganics, Sheer Blend, SPF 50 Mineral Sunscreen Fragrance recalled | Johnson S C and Son | Potency & Assay | Nationwide |
| Drug | CLASS II | Testosterone Gel 1%-dose Packets recalled by Strides PharmaTestosterone | Strides Pharma | Benzene | Nationwide |
| Drug | CLASS I | SinuCleanse Premixed Saline Packets recalled by Ascent Consumer Products | Ascent Consumer Products | Other Bacterial Contamination | Nationwide |
| Drug | CLASS II | fentaNYL Citrate PF 200 mcg recalled by QuVa Pharma | QuVa Pharma | Sterility | Nationwide |
| Drug | CLASS I | SinuCleanse Soft Tip NETI POT Nasal Wash System recalled | Ascent Consumer Products | Other Bacterial Contamination | Nationwide |
| Drug | CLASS I | SinuCleanse Soft Tip Squeeze Bottle Nasal Wash System recalled | Ascent Consumer Products | Other Bacterial Contamination | Nationwide |
| Drug | CLASS II | 8.4% Sodium Bicarbonate Injection, USP, 50 mEq/ (1 mEq/mL) recalledSodium Bicarbonate | Exela Pharma Sciences | Sterility | Nationwide |
| Drug | CLASS II | [Correct Front Panel] Hydrogen Peroxide Topical Solution recalled | Consumer Product Partners | Packaging Defects | VA |
| Drug | CLASS II | fentaNYL Citrate PF 200 mcg recalled by QuVa Pharma | QuVa Pharma | Sterility | Nationwide |
| Drug | CLASS II | Metformin Hydrochloride Extended- Release 500mg recalledMetformin Hydrochloride | A-S Medication Solutions | Packaging Defects | Nationwide |
| Food | CLASS I | Ready-To-Eat Sausage and Bacon Breakfast Sandwiches recalled | Hearthside Food Solutions | Undeclared Sesame | |
| Food | CLASS II | Omni-Macs McDonagh Medical Center Dietary Supplement recalledOmni-Macs McDonagh | Veridance Pharmacal | Other | MO |
| Food | CLASS I | Wangzhine branded Hot Pot Sauce (Spicy) recalledWangzhine | Liaoning Cheng Da (USA) | Undeclared Allergens | CA |
| Food | CLASS I | Glicks Dark Chocolate Conettos, 24 packages recalledGlicks | Kenover Marketing | Undeclared Allergens | 10 states |
| Food | CLASS I | Jinga Glass Noodles with vegetables recalled by HAR MaspethJinga Glass | HAR Maspeth | Undeclared Egg | 10 states |
| Food | CLASS II | favorite day gourmet New York-Style Cheesecake 2 Slices recalled | Dessert Holdings | Undeclared Tree Nuts | 5 states |
| Food | CLASS II | Coffee Roasters Our Family Traverse City Cherry recalled | Massimo Zanetti Beverage U | Labeling Errors | 15 states |
| Food | CLASS I | Wangzhine branded Hot Pot Sauce recalled by Liaoning Cheng Da (USA)Wangzhine | Liaoning Cheng Da (USA) | Undeclared Allergens | CA |
| Food | CLASS III | Flor de Michoacan Blue Hawaiian Artificially Flavored recalledFlor | Paletas Ice Cream | Undeclared Allergens | 4 states |
| Food | CLASS III | Dried Lily Flowers recalled by U.S. Tov | U.S. Tov | Undeclared Sulfites | 30 states |
| Food | CLASS II | Coco-Cola Original Taste recalled by Great Lakes Coca-ColaCoco-Cola | Great Lakes Coca-Cola Distribution | Foreign Material | IL, WI |