| Food | CLASS I | Spaghetti and Chicken Products recalled by Ukrop's Homestyle Foods | Ukrop's Homestyle Foods | Foreign Material | |
| Food | HEALTH ALERT | Chicken Salad Product recalled by Mary's Harvest Fresh | Mary's Harvest Fresh Foods | Listeria | |
| Device | CLASS II | Olympus 4K UHD LCD Monitor recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Medline convenience kits labeled as: Total Joint Kit, Medline Kit recalled | Medline Industries | Other | 8 states |
| Device | CLASS II | Faradrive Steerable Sheath (Clear) - US recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Faradrive Steerable Sheath Clear IDE recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: Neuro Pack, Medline Kit recalled | Medline Industries | Other | 10 states |
| Device | CLASS II | Silent Nite Sleep Appliance recalled by Prismatik Dentalcraft | Prismatik Dentalcraft | Other | Nationwide |
| Device | CLASS II | 3mensio Workstation (Vascular Fenestrated) recalled | PIE Medical Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | SeaSpine Polyaxial Head recalled by Seaspine Orthopedics | Seaspine Orthopedics | Other | Nationwide |
| Device | CLASS II | Faradrive Steerable Sheath Clear Ous recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Device | CLASS II | Emano Flow recalled by Emano Metrics | Emano Metrics | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | TheraSphere 360 Y-90 Management Platform recalled by Boston Scientific | Boston Scientific | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Olympus High Flow Insufflation Unit - UHI recalled | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS I | Medline medical procedure convenience kit labeled as recalled | Medline Industries | Other | CO, IL |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Pipeline Flex Embolization Device with Shield Technology recalled | Micro Therapeutics | Labeling Errors | Nationwide |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | 10 states |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline convenience kits labeled as: C-section, Medline recalled | Medline Industries | Other | 8 states |
| Device | CLASS II | SnapshotGLO Wound Imaging Device recalled by Kent Imaging | Kent Imaging | Device Malfunction | Nationwide |
| Device | CLASS II | Halyard EYE PACK recalled by AVID Medical | Avid Medical | Other | Nationwide |
| Device | CLASS II | The intended use is to be paired with a weapon for aiming purposes recalled | Wilcox Industries | Device Malfunction | Nationwide |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline Anterior Hip, Medline Kit recalled by Medline Industries | Medline Industries | Other | 8 states |
| Device | CLASS II | P28 Phanton Intramedullary Nail System recalled by Paragon 28 | Paragon 28 | Sterility | Nationwide |
| Device | CLASS II | Farastar PFA Generator, Product ID M004PFCE61M460 recalled | Boston Scientific | Other | MN |
| Device | CLASS II | Pipeline Flex Embolization Device with Shield Technology recalled | Micro Therapeutics | Labeling Errors | Nationwide |
| Device | CLASS II | Ventriculostomy Kit recalled by Medtronic Neurosurgery | Medtronic Neurosurgery | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as recalled | Medline Industries | Other | 10 states |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Medline medical convenience kits labeled as: Shoulder Pack recalled | Medline Industries | Other | 10 states |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Power F2 Powered Fastening System recalled by Ferno-Washington | Ferno-Washington | Other | Nationwide |
| Device | CLASS II | Farastar Pulsed Field Ablation Generator, Product ID M004PFCE61M401 recalled | Boston Scientific | Other | MN |
| Device | CLASS II | Medline convenience kits containing Bard¿ Silastic¿ Foley recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Flexible Hystero-Fiberscope Kits recalled by Karl Storz Endoscopy | Karl Storz Endoscopy | Sterility | Nationwide |
| Device | CLASS II | Hotline Fluid Warming Set, single use device recalled by ICU Medical | ICU Medical | Packaging Defects | Nationwide |
| Device | CLASS I | Medline medical procedure convenience kit labeled as recalled | Medline Industries | Other | CO, IL |
| Device | CLASS II | Farastar Ablation Generator EU recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | MiniMed Go App recalled by Medtronic MiniMed | Medtronic MiniMed | Other | Nationwide |
| Device | CLASS II | SafeOp Patient Interface recalled by Alphatec Spine | Alphatec Spine | Device Malfunction | Nationwide |
| Device | CLASS II | System RED 68 Reperfusion Catheter recalled by Penumbra | Penumbra | Other | Nationwide |
| Device | CLASS II | Halyard Standard Line Insertion Pack recalled by AVID Medical | Avid Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Farastar Ablation Generator EU recalled by Boston Scientific | Boston Scientific | Other | MN |
| Device | CLASS II | Faradrive Steerable Sheath Clear recalled by Boston Scientific | Boston Scientific | Other | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Dry Aid (povidone recalledRohto Dry-aid | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 150 mcg (0.0150 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops All-in-one (hypromellose recalledRohto | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS III | Dabigatran etexilate Capsules, 110 mg recalled by Ascend LaboratoriesDabigatran Etexilate | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS I | Cetirizine Hydrochloride Tablets USP 5 mg recalled by JB Chemicals andCetirizine Hydrochloride | JB Chemicals and Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | Rising, Cyproheptadine Hydrochloride Syrup, 2mg recalledCyproheptadine Hydrochloride | Rising Pharma Holding | Particulate Matter | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 50 mcg recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Glycopyrrolate Oral Solution, 1 mg/, delivers recalled by Precision DoseGlycopyrrolate | Precision Dose | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 125 mcg (0.0125 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Glycopyrrolate Injection, USP, 1 mg per (0.2 mg per mL) recalledGlycopyrrolate | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Xylocaine (lidocaine HCl Injection, USP), 1%, 500 mg recalledXylocaine | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Optic Glow recalledRohto Optic Glow | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 112 mcg (0.0112 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 25 mcg recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Amlodipine and Olmesartan Medoxomil Tablets, 10 mg/20 mg recalledAmlodipine And Olmesartan Medoxomil | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS III | Lidolog Kit, Kit Contains: Lidocaine HCl Injection recalledLidolog Kit | Asclemed USA | Other | TN |
| Drug | CLASS II | Divalproex Sodium Delayed-Release Tablets, USP, 500 mg recalledDivalproex Sodium | Bionpharma | Other | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Max Strength recalledRohto | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS II | Lidocaine HCl Injection, USP, 2%, 100 mg recalled by Fresenius Kabi USALidocaine | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 50 mcg (0.050 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Dabigatran etexilate Capsules, 150 mg recalled by Ascend LaboratoriesDabigatran Etexilate | Ascend Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Dry Aid (povidone recalledRohto Dry-aid | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS II | Xylocaine (lidocaine HCl Injection, USP), 1%, 200 mg recalledXylocaine | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Digi Eye (hypromellose recalledRohto Digi-eye | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 25 mcg (0.025 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 125 mcg recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 75 mcg (0.075 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Naropin (ropivacaine hydrochloride Injection, USP) recalledNaropin | Fresenius Kabi USA | Particulate Matter | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 88 mcg (0.088 mg) recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS III | Trokendi XR, topiramate extended-release capsules, 25mg recalled | Supernus Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 150 mcg recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Cool Relief recalledRohto | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 75 mcg recalledLevothyroxine Sodium | Major Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Rohto Cooling Eye Drops Max Strength recalledRohto | Rohto-Mentholatum (Vietnam) | Sterility | Nationwide |
| Food | HEALTH ALERT | Steak Burrito Product recalled by Red'S ALL Natural | Red'S ALL Natural | Undeclared Egg | |
| Food | CLASS I | Fusia, Asian Inspirations, Kimchi & Tofu Kimbap , 6 ea recalledFusia | Gellert Global Group | Undeclared Allergens | 6 states |
| Food | CLASS III | Nautilus Imitation Crab Sticks recalled by Shandong Ling Xian Food CoNautilus Imitation | Shandong Ling Xian Food Co | Undeclared Allergens | CA |
| Food | CLASS I | TNVitamins 100% Organic Moringa Capsules 1,200 mg recalled | Total Nutrition | Salmonella | Nationwide |
| Food | CLASS III | Island Pacific Imitation Crab Sticks recalledIsland Pacific | Shandong Ling Xian Food Co | Undeclared Allergens | CA |
| Food | CLASS III | Island Pacific Imitation Crab Flakes recalledIsland Pacific | Shandong Ling Xian Food Co | Undeclared Allergens | CA |
| Food | CLASS I | Modern Warrior Ready, Dietary Supplement recalledModern Warrior | Modern Warrior Life | Hidden Drug Ingredients | Nationwide |
| Food | CLASS II | Root Beer Syrup recalled by Vintage RootsVintage Roots | Vintage Roots | Foreign Material | MT |
| Food | CLASS II | Wonton Wrappers packed into and sold as bags)/case recalled by Man FonWonton Wrappers | Man Fon | Undeclared Wheat & Gluten | CA, NM |
| Food | CLASS II | Won Ton Wrappers Extra Thin recalled by Man FonMan Fon | Man Fon | Undeclared Allergens | CA, NM |
| Food | CLASS II | Brooklyn Roasting Company Pasteurized Cold Brew recalledBrooklyn Roasting | Brooklyn Roasting Works | Botulism | NJ, NY |
| Food | CLASS I | Organic Moringa Powder recalled by Green Jeeva | Green Jeeva | Salmonella | CA |
| Food | CLASS I | Not Ready-To-Eat (NRTE) Bacon Product recalled by Maple Leaf Foods | Maple Leaf Foods | Foreign Material | |
| Food | CLASS I | Chicken Noodle Soup Product recalled by BCI Foods | BCI Foods | Processing Deviation | |
| Device | CLASS I | Introducer Kit, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS I | Bone Marrow Tray recalled by Argon Medical Devices | Argon Medical Devices | Sterility | Nationwide |
| Device | CLASS I | Impella CP Smart Assist Set, JP, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS I | Intro Kitand, PKGD, JP, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS I | Impella 5.5 Smart Assist Set, JP, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS I | Abiomed REF: 0052-3006, Introducer Kit for Impella Hemostatic Peel recalled | Oscor | Packaging Defects | MA |
| Device | CLASS I | Impella CP Set, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Rio" II Nasal Pillows Interface recalled by 3B Medical | 3B Medical | Packaging Defects | Nationwide |
| Device | CLASS I | Impella RP Flex with SmartAssist Set, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Medtronic DLP One-Piece Pediatric Arterial Cannula recalled | Medtronic Perfusion Systems | Foreign Material | Nationwide |
| Device | CLASS II | da Vinci SP Instrument Arm Drape, SP recalled by Intuitive Surgical | Intuitive Surgical | Other | Nationwide |
| Device | CLASS II | Medline Kits containing Zimmer Biomet mixing bowls recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Olympus Toomey Evacuator 50cc with Adaptor recalled | Olympus Corporation of the Americas | Sterility | Nationwide |
| Device | CLASS II | Orthofix Minirail, Short, Lengthener recalled by Orthofix U.S | Orthofix U.S | Labeling Errors | 22 states |
| Device | CLASS II | Optima XR240amx, Mobile Digital Radiographic System recalled | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | The Vasoview Hemopro 2 Endoscopic Vessel Harvesting System recalled | Maquet Cardiovascular | Sterility | Nationwide |
| Device | CLASS I | Impella 5.5 SmartAssist S2 Set, JP, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS I | T-Lok Bone Marrow Tray recalled by Argon Medical Devices | Argon Medical Devices | Sterility | Nationwide |
| Device | CLASS II | Medtronic Bio-Medicus Adult Cannula Kit recalled | Medtronic Perfusion Systems | Foreign Material | Nationwide |
| Device | CLASS I | Impella CP Introducer Kit, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Orthofix Minirail, Articulated, Fixator, Vertical Axis recalled | Orthofix U.S | Labeling Errors | 22 states |
| Device | CLASS I | Impella CP Set, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Kits containing Zimmer Biomet mixing bowls recalled | Medline Industries | Sterility | Nationwide |
| Device | CLASS II | Orthofix Articulated Minirail Fixator Horizontal Axis recalled | Orthofix U.S | Labeling Errors | 22 states |
| Device | CLASS I | One-Piece Introducer Tray recalled by Argon Medical Devices | Argon Medical Devices | Sterility | Nationwide |
| Device | CLASS II | Plum Solo Precision IV Pump, v1.0.3 recalled by ICU Medical | ICU Medical | Other | Nationwide |
| Device | CLASS I | Abiomed REF: 0052-3021, Introducer Kit for Impella Hemostatic Peel recalled | Oscor | Packaging Defects | MA |
| Device | CLASS I | Transvenous Pacing Electrode Tray w/ Bipolar Balloon Pacing recalled | Argon Medical Devices | Sterility | Nationwide |
| Device | CLASS I | Insertion Kit, Pkgd, JP, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Photera 600, phototherapy device recalled by Daavlin Distributing | Daavlin Distributing | Device Malfunction | Nationwide |
| Device | CLASS I | Arterial Line Kit recalled by Argon Medical Devices | Argon Medical Devices | Sterility | Nationwide |
| Device | CLASS II | Olympus Glass Body for 194 Ellik Evacuator recalled | Olympus Corporation of the Americas | Sterility | Nationwide |
| Device | CLASS II | Olympus Toomey Evacuator 30cc with Adaptor recalled | Olympus Corporation of the Americas | Sterility | Nationwide |
| Device | CLASS II | ST Aia-Pack Testosterone, IN Vitro Diagnostic Use Only recalled | Tosoh Bioscience | Potency & Assay | Nationwide |
| Device | CLASS I | General Biospy Tray recalled by Argon Medical Devices | Argon Medical Devices | Sterility | Nationwide |
| Device | CLASS II | Optima XR220amx, Mobile Digital-Ready Radiographic System recalled | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Photera 400, phototherapy device recalled by Daavlin Distributing | Daavlin Distributing | Device Malfunction | Nationwide |
| Device | CLASS I | Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel recalled | Oscor | Packaging Defects | MA |
| Device | CLASS II | Olympus Ellik Evacuator Includes Glass Body recalled | Olympus Corporation of the Americas | Sterility | Nationwide |
| Device | CLASS I | Impella CP Introducer Kit, 13 and, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Optima XR200amx, Mobile Digital-Ready Radiographic System recalled | GE Medical Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Photera 600 3-D, phototherapy device recalled by Daavlin Distributing | Daavlin Distributing | Device Malfunction | Nationwide |
| Device | CLASS I | Impella CP Introducer Kit, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Replacement Brush Heads recalled by Papablic | Papablic | Device Malfunction | Nationwide |
| Device | CLASS II | Replacement Brush Heads recalled by Papablic | Papablic | Device Malfunction | Nationwide |
| Device | CLASS I | Impella CP Set, Pump Set recalled by Abiomed | Abiomed | Packaging Defects | Nationwide |
| Device | CLASS II | Rapid Refill Continuous Injection System, UPN M00566001 recalled | Boston Scientific | Packaging Defects | Nationwide |
| Device | CLASS II | Orthofix Minirail, Standard Lengthener recalled by Orthofix U.S | Orthofix U.S | Labeling Errors | 22 states |
| Drug | CLASS II | Foster & Thrive, Carbamide Peroxide recalled by Bell Pharmaceuticals | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Good Neighbor Pharmacy, Carbamide Peroxide 6.5%, a) Kit recalledGood Neighbor Pharmacy Earwax Removal | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Audiologist's Choice, Carbamide Peroxide 6.5% a) Kit recalledAudiologists Choice Earwax Removal System | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | TopCare Health, Carbamide Peroxide 6.5% a) Kit recalledTopcare Earwax Removal Kit | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | CVS Health, Carbamide Peroxide, 6.5%, a) Bottle recalledCvs Health Earwax Removal Drops Earwax Removal Aid | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | meijer, Carbamide Peroxide 6.5%, Washer Bulb included recalledMeijer Earwax Removal Kit | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Nystatin Cream USP, (100,000 USP Nystatin Units) recalled by Padagis USNystatin | Padagis US | Potency & Assay | Nationwide |
| Drug | CLASS II | CAREone, Carbamide Peroxide recalled by Bell PharmaceuticalsCareone Earwax Removal Drops | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Family Wellness, Carbamide Peroxide 6.5%, Kit recalledFamily Wellness Earwax Removal Earwax And Bulb | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Leader, Carbamide Peroxide recalled by Bell PharmaceuticalsLeader Earwax Removal Kit Earwax Removal Aid And Bulb | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Clinere, Carbamide Peroxide recalled by Bell PharmaceuticalsClinere Ear Wax Remover | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | QC Quality Choice, Carbamide Peroxide recalled by Bell PharmaceuticalsQuality Choice Earwax Removal Kit | Bell Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | Cleviprex (clevidipine injectable emulsion) 50 mg recalled by Chiesi USACleviprex | Chiesi USA | Sterility | Nationwide |
| Food | CLASS I | Ice Pop, D'Dioses Guayaba recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | Pillsbury Bread Rolls, Kaiser Roll Dough recalledPillsbury | General Mills James Ford Bell Technical Center | Foreign Material | 19 states |
| Food | CLASS II | Pillsbury Bread Rolls, Hard Roll Dough recalledPillsbury | General Mills James Ford Bell Technical Center | Foreign Material | 19 states |
| Food | CLASS I | Ice Pop, D'Dioses Rompope recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | Winfield's CWB Chocolate Bar recalled by Chocolate Bar HoldingsWinfield's CWB | Chocolate Bar Holdings | Undeclared Milk | TX |
| Food | CLASS I | Ice Pop, D'Dioses Coconut recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | WY Duck Sauce, flexible film packets, 500 packets recalledWY Duck | W.Y. Industries | Foreign Material | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Vainilla recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Grocella recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Mamey recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | Amy's Organic Soups Lentil Light IN Sodium recalled by Amy's KitchenAmy's | Amy's Kitchen | Mold | 28 states |
| Food | CLASS I | Ice Pop, D'Dioses Nanche recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | functional formularies Nourish Organic Whole Foods Meal recalled | Nutricia North America | Potency & Assay | 49 states |
| Food | CLASS I | Ice Pop, D'Dioses Pina Colada recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Organic Whole Blueberries recalled by Frutas y Hortalizas del Sur | Frutas y Hortalizas del Sur | E. coli | FL |
| Food | CLASS I | Ice Pop, D'Dioses Pistachio recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Cookies Cream recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Limon recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Mango recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Fresa Leche recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | Ruby, Artichoke Hearts Quartered Drained WT, Store in dry conditions recalledRuby | Gellert Global Group | Foreign Material | 4 states |
| Food | CLASS II | Ola-ola Pounded Groundnuts (intwilo) recalled by FayusOla-ola Pounded | Fayus | Undeclared Peanuts | TX |
| Food | CLASS I | Ice Pop, D'Dioses Arroz con Leche recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS II | functional formularies Liquid Hope Organic Whole Foods Meal recalled | Nutricia North America | Potency & Assay | 49 states |
| Food | CLASS I | Ice Pop, D'Dioses Tamarindo recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Food | CLASS I | Ice Pop, D'Dioses Nuez recalled by D'Dioses Fruit Pops | D'Dioses Fruit Pops | Undeclared Milk | 4 states |
| Device | CLASS II | OmniTract Surgical Retractor System recalled | Integra LifeSciences Corp. (NeuroSciences) | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Open Heart Peds Pack recalled | Medline Industries | Temperature Abuse | Nationwide |
| Device | CLASS II | Empowr 3d Knee Ins, Ve recalled by Encore Medical | Encore Medical | Packaging Defects | 14 states |
| Device | CLASS II | Empowr 3d Knee Ins, Ve recalled by Encore Medical | Encore Medical | Packaging Defects | 14 states |
| Device | CLASS II | Medline Convenience Kits: Open Heart Peds Pack recalled | Medline Industries | Temperature Abuse | Nationwide |
| Device | CLASS II | Intracept Access Instruments, Description recalled by Boston Scientific | Boston Scientific Neuromodulation | Sterility | Nationwide |
| Device | CLASS II | Vitek 2 Ast-N447 Test Kit Product reference recalled by Biomerieux | Biomerieux | Other | MO |
| Device | CLASS II | Tmini Femur Tracking Array recalled by Think Surgical | Think Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Geneva Brachytherapy Applicator recalled by Elekta | Elekta | Other | Nationwide |
| Device | CLASS II | Brachytherapy Applicator Advanced Gynecological Applicator recalled | Elekta | Other | Nationwide |
| Device | CLASS II | 5008X Blood Tubing Set recalled by Fresenius Medical Care | Fresenius Medical Care Holdings | Other | Nationwide |
| Device | CLASS II | Fletcher CT/MR Shielded Applicator Set Intracavitary Remote recalled | Elekta | Other | Nationwide |
| Device | CLASS II | Atellica CH Enzymatic Hemoglobin A1c (A1c_E) recalled | Siemens Healthcare Diagnostics | Potency & Assay | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Anesthesia Kit Peds 90-LF recalled | Medline Industries | Temperature Abuse | Nationwide |
| Device | CLASS II | Versius Surgical System US Vesius Surgeon Console US recalled | CMR Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Olympus Single Use Distal Cover recalled by Olympus Corporation of the | Olympus Corporation of the Americas | Other | Nationwide |
| Device | CLASS II | MiniMed Insulin Pump recalled by Medtronic MiniMed | Medtronic MiniMed | Device Malfunction | CA |
| Device | CLASS II | KL Owen Custom Orthodontic Solution recalled by Klowen Braces | Klowen Braces | Device Malfunction | Nationwide |
| Device | CLASS II | GSP Neonatal GALT Kit recalled by Wallac Oy | Wallac OY | Potency & Assay | Nationwide |
| Device | CLASS II | Aquacel Ag Surgical SP recalled by ConvaTec | ConvaTec | Potency & Assay | Nationwide |
| Drug | CLASS II | Methohexital Sodium, 100 mg/ (10 mg/mL), Total Volume recalled | QuVa Pharma | Potency & Assay | Nationwide |
| Drug | CLASS II | Drogueria San Juan Puerto Rico Isopropyl Alcohol recalled | Gasco Industrial | Potency & Assay | Nationwide |
| Drug | CLASS II | Medline Remedy Specialized Silicone Cream (Hydraguard-D ) recalled | BioMed Laboratories | Potency & Assay | Nationwide |
| Drug | CLASS II | Azacitidine for Injection 100mg/Vial-Dose Vial recalled | Reliance Life Sciences Private | Sterility | Nationwide |
| Drug | CLASS II | Pemetrexed for Injection 100mg/Vial-Dose Vial recalled | Reliance Life Sciences Private | Sterility | Nationwide |
| Drug | CLASS II | Bortezomib for Injection 3.5mg/Vial per Single-Dose Vial recalled | Reliance Life Sciences Private | Sterility | Nationwide |
| Drug | CLASS II | Drogueria San Juan Puerto Rico Isopropyl Alcohol recalled | Gasco Industrial | Potency & Assay | Nationwide |
| Drug | CLASS II | Gasco Isopropyl Alcohol 70%, Net Contents recalled by Gasco Industrial | Gasco Industrial | Potency & Assay | Nationwide |
| Drug | CLASS II | Pemetrexed for Injection 500mg/Vial-Dose Vial recalled | Reliance Life Sciences Private | Sterility | Nationwide |
| Drug | CLASS II | Clomiphene Citrate USP Active Pharmaceutical Ingredient recalled | Shimoga Chemicals | Manufacturing (CGMP) Deviations | CA, FL |
| Drug | CLASS II | Drogueria San Juan Puerto Rico Isopropyl Alcohol recalled | Gasco Industrial | Potency & Assay | Nationwide |
| Drug | CLASS II | Gasco Isopropyl Alcohol 70% Gasco Industrial Corp. recalled | Gasco Industrial | Potency & Assay | Nationwide |
| Drug | CLASS II | Gasco Isopropyl Alcohol 70%, Net Contents: 1 US Gallon recalled | Gasco Industrial | Potency & Assay | Nationwide |
| Drug | CLASS II | Methohexital Sodium for Injection, USP 500 mg Multiple Dose Vial recalledMethohexital Sodium | Onesource Specialty Pharma | Potency & Assay | Nationwide |
| Food | CLASS II | Johnny's Salad and Pasta Elegance recalled by Adams Extract & SpiceJohnny's | Adams Extract & Spice | Undeclared Sesame | TX |
| Food | CLASS I | Fresh to You Burger Chicken Fillet Deluxe with Bacon recalled | Fresh & Ready Foods | Salmonella | OR, WA |
| Food | CLASS I | High Valley Orchard Chocolate Covered Raisins recalledHigh Valley | Lehi Valley Trading Company | Undeclared Peanuts | Nationwide |
| Food | CLASS I | JB Chicken Sknls 35.73# recalled by Adams Extract & Spice | Adams Extract & Spice | Undeclared Sesame | TX |
| Food | CLASS II | Alabama Banana Pudding Marshmallow of individual marshmallows recalledAlabama | Wondermade | Foreign Material | 4 states |
| Food | CLASS I | Fresh to You Burger Chicken Fillet recalled by Fresh & Ready Foods | Fresh & Ready Foods | Salmonella | OR, WA |
| Food | CLASS I | Coopers Bbq Bean Mix recalled by Adams Extract & SpiceCoopers Bbq | Adams Extract & Spice | Undeclared Sesame | TX |
| Food | CLASS II | Vanilla Dessert Shells (Giant), 6 dessert shells/1 package recalled | Specialty Bakers | Undeclared Allergens | PA |
| Food | CLASS I | Organic Moringa Leaf Powder recalled by Trafa PharmaceuticalPharmaceuticals Inc | Trafa Pharmaceutical | Salmonella | NY |
| Food | CLASS II | Wise Onion Rings recalledWise | Wise Foods | Undeclared Allergens | 7 states |
| Food | CLASS I | EC Hot Links Seasoning 45.05# recalled by Adams Extract & Spice | Adams Extract & Spice | Undeclared Sesame | TX |
| Food | CLASS II | Bakr Brown Butter Chocolate Chunk Ready to Bake Cookie recalledBakr Brown | Bear Stewart | Undeclared Soy | 4 states |
| Food | CLASS I | Smoked Sausage Spice 32.86# recalled by Adams Extract & Spice | Adams Extract & Spice | Undeclared Sesame | TX |
| Device | CLASS I | Hillrom Volara P.Circuit 5KIT (System Single Patient Use Circuit) recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: L&d Continuous Epidural Tray recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Multimed, Cvc Bundle recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS I | Hillrom Volara System P.Circuit Kit (Single Patient Use Circuit) recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | Artis icono ceiling recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | 5605150 Power-Trialysis Short-Term Straight Dialysis recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS I | Omnipod (Eros) Pod recalled by Insulet | Insulet | Packaging Defects | Nationwide |
| Device | CLASS II | IntelliCuff, Portable automatic cuff pressure controller recalled | Hamilton Medical | Packaging Defects | Nationwide |
| Device | CLASS II | Medline 111 Gravity Set W/3 Needle Free Y-Sites recalled | BD Switzerland Sarl | Other | IL |
| Device | CLASS II | Short Monobloc Stem Broaches, Size recalled by Medacta Usa | Medacta Usa | Device Malfunction | Nationwide |
| Device | CLASS II | CRE Pro Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Sterile Tourniquet Hoses A.T.S¿ 4000 TS Tourniquet Systems recalled | Zimmer Surgical | Sterility | Nationwide |
| Device | CLASS I | A M S, Aligned Medical Solutions, Preop Kit-NS recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS I | A M S, Aligned Medical Solutions, Dsaek Pack-RX recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS II | 1174108 PowerPICC Catheter Single-Lumen recalled by Bard Access Systems | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | CRE Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Solar GI System (Water Perfusion) recalled | Laborie Medical Technologies | Device Malfunction | Nationwide |
| Device | CLASS I | Reprocessed Electrophysiology Catheters and Ultrasound Catheters recalled | Medline Industries | Particulate Matter | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Mercy Medical Circumcision Tray recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Arterial Line Kit recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Artis icono biplane recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS I | Medtronic Harmony Delivery Catheter System recalled | Medtronic Heart Valves Division | Other | Nationwide |
| Device | CLASS II | 4380 Economy Soft Tissue Biopsy Tray recalled by Bard Access Systems | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | CRE Pro Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Radius VSM Disposable NIBP Cuff recalled by Masimo | Masimo | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Ophthalmic Pack W/Lido recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Cyberknife Treatment Deliver System equipped recalled | Accuray | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters CV recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Depuy Synthes, Attune Revision Hinge Knee Hinge Housing recalled | Depuy (Ireland) | Sterility | MN, NC, TX |
| Device | CLASS II | CRE Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | CK000980A PowerMidline Catheter Dual-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | CRE Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | 7617408 Groshong NXT ClearVue Catheter Single-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS I | Hillrom Volara System P.Circuit 5KIT AC recalled by Baxter Healthcare | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS I | A M S, Aligned Medical Solutions, Thyroid Fna Pack-RX recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS II | Otp5000 Thora/para Tray, Non-valved recalled by Bard Access Systems | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | Depuy Synthes, Attune Revision Hinge Knee Hinge Insert recalled | Depuy (Ireland) | Sterility | MN, NC, TX |
| Device | CLASS II | Artis icono floor recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | Sterile Tourniquet Hoses A.T.S¿ 4000 TS Tourniquet Systems recalled | Zimmer Surgical | Sterility | Nationwide |
| Device | CLASS I | A M S, Aligned Medical Solutions, Dr. Lewin Pack recalled | Windstone Medical Packaging | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Block Tray recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | CRE Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | CRE Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Lumbar Puncture Choice recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS I | Omnipod DASH Pod recalled by Insulet | Insulet | Packaging Defects | Nationwide |
| Device | CLASS II | Adapter for Head Positioning recalled by Baxter Healthcare | Baxter Healthcare | Other | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Cyberknife Treatment Deliver System equipped recalled | Accuray | Device Malfunction | Nationwide |
| Device | CLASS II | CK000662 PowerPICC SOLO HF Catheter Triple-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | CRE Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS I | Breathing circuit set, coaxial recalled by Hamilton Medical AG | Hamilton Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Arterial Access Tray W/Lidocaine recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | CRE Pro Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component recalled | W L Gore & Associates | Other | Nationwide |
| Device | CLASS II | Syringe Luer Lok 10cc-200/box Bd recalled by Mentor Texas | Mentor Texas | Device Malfunction | CA, FL, PA |
| Device | CLASS II | Shiley Disposable Decannulation Plug recalled by Covidien | Covidien | Other | Nationwide |
| Device | CLASS II | CRE Pro Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | 1274108D PowerPICC SV Catheter Dual-Lumen REKW2449 recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | ENFit ExSet Strl 60 PV EN recalled by Medela | Medela | Device Malfunction | 18 states |
| Device | CLASS II | Artis icono ceiling recalled by Siemens Medical Solutions USA | Siemens Medical Solutions USA | Other | Nationwide |
| Device | CLASS II | CRE Pro Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | RayCare 2024A SP4 recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Pain Mgmt/ Pref W. Med Ndl recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS I | Hillrom Volara System P.Circuit Kit AC (Single Patient Use Circuit) recalled | Baxter Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | CK000525B PowerPICC Provena SOLO Catheter Dual-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | 5625240 DuoGlide Short-Term Straight Dialysis Catheter Dual-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | CK000880 Provena Midline Catheter Dual-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Suturing SET recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Medline Convenience Kits: PI CVC KIT recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | CK000727 PowerMidline Catheter Single-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS I | Omnipod 5 Pods recalled by Insulet | Insulet | Packaging Defects | Nationwide |
| Device | CLASS II | Zeiss Intrabeam Spherical Applicator recalled by Carl Zeiss Meditec AG | Carl Zeiss Meditec | Other | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Imaging Biopsy Tray recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Std, Intro-flex Introducer 6F recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | 5855240 Power-Trialysis Slim-Cath Straight Short-Term recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | Radius VSM ECG pre-connected Set recalled by Masimo | Masimo | Device Malfunction | Nationwide |
| Device | CLASS II | Medline Convenience Kits: Suture Tray recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Pilling Wecksorb Neurosponges recalled by Teleflex | Teleflex | Device Malfunction | Nationwide |
| Device | CLASS II | CRE Pro Wireguided recalled by Boston Scientific | Boston Scientific | Sterility | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | CK000495A Poly Midline Catheter Single-Lumen recalled | Bard Access Systems | Other | Nationwide |
| Device | CLASS II | RayCare 2024A SP1 recalled by Raysearch Laboratories Ab | Raysearch Laboratories AB | Other | Nationwide |
| Device | CLASS II | Medline Convenience kits containing Swan-Ganz Catheters Kit recalled | Medline Industries | Packaging Defects | Nationwide |
| Device | CLASS II | GC Agar Base R04030 recalled by Remel | Remel | Other | Nationwide |
| Drug | CLASS II | Synjardy XR Tablets (empagliflozin recalled by Boehringer Ingelheim | Boehringer Ingelheim Pharmaceuticals | Manufacturing (CGMP) Deviations | OH |
| Drug | CLASS II | Dextroamphetamine Saccharate recalled by Lannett CompanyDextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate And Amphetamine Sulfate | Lannett | Packaging Defects | Nationwide |
| Drug | CLASS II | BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate (CHG) recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | BD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Gemcitabine Injection per (38 mg/mL) Single-Dose Vial recalledGemcitabine | McKesson | Temperature Abuse | Nationwide |
| Drug | CLASS II | BD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Terpenicol Antifungal Cream (Undecylenic Acid 13%) recalledTerpenicol | Blaine Labs | Potency & Assay | Nationwide |
| Drug | CLASS II | Trifluent Pharma Tridergel Wound Care Gel recalled by Blaine LabsTridergel | Blaine Labs | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Imuldosa, (ustekinumab-srlf) Injection, 130 mg/ (5mg/mL) recalledImuldosa | Accord Biopharma | Sterility | Nationwide |
| Drug | CLASS II | Lidocaine HCl Injection USP, 1% (10 mg/mL) single dose ampule recalledLidocaine Hydrochloride | Asclemed USA | Sterility | Nationwide |
| Drug | CLASS II | vite20 Antifungal Cream, (10% Undecylenic Acid) recalled by Blaine Labs | Blaine Labs | Potency & Assay | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 60 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 90 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | BD PurPrep, (Povidone-iodine 8.3% w/w recalled by CareFusion 213Purprep | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Levothyroxine Sodium Tablets, USP, 300 mcg (0.3mg) recalledLevothyroxine Sodium | Accord Healthcare | Potency & Assay | Nationwide |
| Drug | CLASS II | BD ChloraPrep Scrub Teal, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Revitaderm Wound Care, First Aid Antiseptic Gel recalled by Blaine LabsRevitaderm Wound Care | Blaine Labs | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | prednisoLONE Acetate Ophthalmic Suspension recalledPrednisolone Acetate | Lupin Pharmaceuticals | Other | Nationwide |
| Drug | CLASS II | BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Tripenicol S Antifungal Solution (Undecylenic Acid 25%) recalledTripenicol S | Blaine Labs | Potency & Assay | Nationwide |
| Drug | CLASS III | Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine recalled | SUN Pharmaceutical Industries | Potency & Assay | Nationwide |
| Drug | CLASS I | Revitaderm Wound Care Gel, Benzalkonium Chloride recalled by Blaine Labs | Blaine Labs | Sterility | Nationwide |
| Drug | CLASS II | BD ChloraPrep CLear, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Accucaine, Kit contains: Lidocaine HCl Injection recalledAccucaine | Asclemed USA | Sterility | Nationwide |
| Drug | CLASS II | Cinacalcet Hydrochloride Tablets, 30 mg recalled by Cipla USACinacalcet | Cipla USA | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Glucagon Emergency Kit for Low Blood Sugar, Glucagon recalledGlucagon | Lupin Pharmaceuticals | Potency & Assay | Nationwide |
| Drug | CLASS II | ChloraPrep Frepp, Clear, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Fungal Fusion Eradication Solution, Antifungal & Antimicrobial Kit recalled | Blaine Labs | Potency & Assay | Nationwide |
| Drug | CLASS II | BD ChloraPrep Hi-Lite Orange recalled by CareFusion 213Chloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Terpenicol Antifungal Solution, (Undecylenic recalled by Blaine LabsTerpenicol | Blaine Labs | Potency & Assay | Nationwide |
| Food | CLASS II | Plastic clear pail blue label which reads recalled by Wells EnterprisesPlastic | Wells Enterprises | Foreign Material | WI |
| Food | CLASS II | MorningStar Farms Hot & Spicy Sausage Patties recalled by Mars SnackingMorningStar | Mars Snacking | Foreign Material | 41 states |
| Food | CLASS I | a.) nara organics Whole Milk Organic Infant Formula recalled | Nara Organics | Botulism | Nationwide |
| Food | CLASS II | Ocular Plus with Lutein, Zeaxanthin, and Omega recalledOcular Plus | Provision Health | Undeclared Allergens | CA |
| Food | CLASS II | Vista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAX | Provision Health | Undeclared Allergens | CA |
| Food | CLASS I | First Street Dark Chocolate Raisins recalledFirst Street | Western Mixers Produce & Nuts | Undeclared Peanuts | CA |
| Food | CLASS I | Mogo Pure Moringa Oleifera Capsules, Herbal Supplement recalledMogo | MOGO Moringa | Salmonella | Nationwide |
| Food | CLASS II | Pepperoni Rolls recalled by Fry Pie FactoryPepperoni Rolls | Fry Pie Factory | Undeclared Allergens | OH, WV |
| Food | CLASS II | MorningStar Farms Buffalo Chik'n Nuggets recalled by Mars SnackingMorningStar | Mars Snacking | Foreign Material | 41 states |
| Food | HEALTH ALERT | A Ready-To-Eat Beef Jerky Product recalled by GoodTimes Beef Jerky | GoodTimes Beef Jerky | Undeclared Wheat & Gluten | |
| Device | CLASS II | Philips Telemetry Monitor 5500 1.4 GHz recalled by Philips North America | Philips North America | Device Malfunction | Nationwide |
| Device | CLASS II | Off-Axis Comprehensive Shoulder System, Large, Augment recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Surgify Halo, Long recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Long recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Off-Axis Comprehensive Shoulder System Small, Augment recalled by Zimmer | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Hexalob Screw various sizes recalled by Acumed | Acumed | Device Malfunction | Nationwide |
| Device | CLASS II | Off-Axis Alliance Glenoid, Left, 4-Peg, Augment, Reamer Guide recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS I | Impella CP Set with SmartAssist (10th Generation) recalled by Abiomed | Abiomed | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Short recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Short recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Extendable recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Long recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Foreign Material | Nationwide |
| Device | CLASS II | Surgify Halo, Medium recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS I | Medline Convenience Kits: Open Heart Cds recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | TMJ Bilateral Implants recalled by TMJ Solutions | TMJ Solutions | Other | Nationwide |
| Device | CLASS I | Medline Convenience Kits: Drawer 6 Central Line Insertio recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Surgify Halo, Extendable recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Short recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Avalon Fetal Monitor, FM 30 Part numberM2703A recalled | Philips North America | Other | Nationwide |
| Device | CLASS II | Octopus Evolution Tissue Stabilizer recalled | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | GE Healthcare AW Server 3.2 ext.6.5 recalled by GE Medical Systems SCS | GE Medical Systems SCS | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Long recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS I | Medline Convenience Kits: Drawer 6A Adult Central Line recalled | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Extendable recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Multi-Snare Set recalled by Pfm Medical | PFM Medical | Other | Nationwide |
| Device | CLASS I | Medline Convenience Kits recalled by Medline Industries | Medline Industries | Processing Deviation | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Long recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS I | Low Profile Introducer Kit for Impella CP. Impella Set recalled | Abiomed | Other | Nationwide |
| Device | CLASS II | Persona Revision¿ Trabecular Metal¿ Femoral Distal Augment recalled | Zimmer | Packaging Defects | IN |
| Device | CLASS II | Thuvera Laser Console recalled by IPG Medical | IPG Medical | Device Malfunction | Nationwide |
| Device | CLASS II | Intera Oncology Intera 3000 Hepatic Artery Infusion Pump recalled | Boston Scientific | Packaging Defects | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Short recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Octopus 4 Tissue Stabilizer recalled by Medtronic Perfusion Systems | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | Da Vinci ASSY, PSS, SP1098 recalled by Intuitive Surgical | Intuitive Surgical | Device Malfunction | Nationwide |
| Device | CLASS II | Inzone Detachment System recalled by Stryker Neurovascular | Stryker Neurovascular | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Extendable recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS I | Low Profile Introducer Kit for Impella CP. Impella Set recalled | Abiomed | Other | Nationwide |
| Device | CLASS II | Off-Axis Alliance Glenoid, Right, 4-Peg, Augment, Reamer Guide recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Octopus Evolution AS Tissue Stabilizer recalled | Medtronic Perfusion Systems | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Long recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Surgify Halo, Short recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | Philips Avalon Fetal Monitor, FM20 recalled by Philips North America | Philips North America | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Surgify Halo, Short recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS I | Impella CP Set with SmartAssist (10th Generation) recalled by Abiomed | Abiomed | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Convenience kits containing select SKUs of Polycarbonate recalled | Medline Industries | Other | Nationwide |
| Device | CLASS II | Vocsn+Pro package recalled by Ventec Life Systems | Ventec Life Systems | Device Malfunction | Nationwide |
| Device | CLASS II | Off-Axis Comprehensive Shoulder System, Medium, Augment recalled | Zimmer | Foreign Material | Nationwide |
| Device | CLASS II | Surgify Halo, Extendable recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Device | CLASS II | G7 Continuous Glucose Monitoring System Dexcom G7 US Retail recalled | Dexcom | Device Malfunction | CA |
| Device | CLASS II | Surgify Halo, Medium recalled by Surgify Medical Oy | Surgify Medical OY | Device Malfunction | Nationwide |
| Drug | CLASS I | BD ChloraPrep Frepp Clear,(2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Sensipar (cinacalcet) Tablets, 30mg recalled by AmgenSensipar | Amgen | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Sensipar (cinacalcet) Tablets, 90mg recalled by AmgenSensipar | Amgen | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Perampanel CIII Tablets, 6mg recalled by Sun Pharmaceutical IndustriesPerampanel | SUN Pharmaceutical Industries | Packaging Defects | Nationwide |
| Drug | CLASS III | hydrOXYzine Hydrochloride Oral Solution, USP, 10 mg/ (1 Pint) recalledHydroxyzine Hydrochloride | ANI Pharmaceuticals | Other | Nationwide |
| Drug | CLASS I | BD ChloraPrep Clear (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Vitamin See Antioxidant Preservative Free Eye Drops recalled by PReye | PReye | Sterility | CO |
| Drug | CLASS II | Carton Label: Major, Methylergonovine Maleate Tablets recalledMethylergonovine Maleate | The Harvard Drug Group | Potency & Assay | Nationwide |
| Drug | CLASS II | Total Parental Nutrition - Pediatric PN Patient-Specific recalled | Central Admixture Pharmacy Services | Packaging Defects | MA |
| Drug | CLASS II | BD ChloraPrep Frepp Clear, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Duloxetine D/R, a) 30 mg recalled by Direct Rx | Direct Rx | Nitrosamine Impurity | Nationwide |
| Drug | CLASS II | Povi-One, 10% Povidone-Iodine Oral Antiseptic recalledPovi-one | Elevate Oral Care | Potency & Assay | Nationwide |
| Drug | CLASS II | Sensipar (cinacalcet) Tablets, 60mg recalled by AmgenSensipar | Amgen | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Fenofibrate Capsules, USP 200 mg recalled by Ajanta Pharma USAFenofibrate | Ajanta Pharma USA | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | BD ChloraPrep Clear, (2% w/v chlorhexidine gluconate recalledChloraprep One-step | CareFusion 213 | Sterility | Nationwide |
| Drug | CLASS II | Corlanor (ivabradine) tablets, 5 mg recalled by AmgenCorlanor | Amgen | Packaging Defects | Nationwide |
| Drug | CLASS II | Corlanor (ivabradine) tablets, 7.5mg recalled by AmgenCorlanor | Amgen | Other | Nationwide |
| Drug | CLASS II | Lacosamide Tablets, USP, C V, 100mg recalled by Annora Pharma PrivateLacosamide | Annora Pharma Private | Packaging Defects | Nationwide |
| Food | CLASS I | Sunflower Seeds Salted recalled by George J Howe CompanySunflower | George J Howe Company | Undeclared Tree Nuts | 25 states |
| Food | CLASS II | boichik bagles Tuna Salad Ingredients: albacore tuna recalled | Boichik Bagels | Undeclared Egg | CA |
| Food | CLASS II | Joy Peach Lassi recalled by Joy Gourmet FoodsJoy Peach | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS II | Joy Salty Lassi recalled by Joy Gourmet FoodsJoy Salty | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | 5# Sunflower Seeds C/NS recalled by George J Howe Company | George J Howe Company | Undeclared Tree Nuts | 25 states |
| Food | CLASS I | Zapp's Brand Bayou Blackened Ranch Potato Chips recalledZapp's | Utz Quality Foods | Salmonella | 34 states |
| Food | CLASS II | Joy Mint Lassi recalled by Joy Gourmet FoodsJoy Mint | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Pecan Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS II | Whitefish Salad Ingredients: Smoked whitefish, mayonnaise recalled | Boichik Bagels | Undeclared Egg | CA |
| Food | CLASS I | Spring & Mulberry Pure Dark Date-Sweetened Chocolate recalled | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS I | Tub Nut - Sunflower Seed recalled by George J Howe CompanyTub | George J Howe Company | Undeclared Tree Nuts | 25 states |
| Food | CLASS I | 5# Sunflower Seeds C/S recalled by George J Howe Company | George J Howe Company | Undeclared Tree Nuts | 25 states |
| Food | CLASS II | Joy Orange Lassi recalled by Joy Gourmet FoodsJoy | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Blood Orange Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS I | Pearl Milling Company Original Pancake & Waffle Mix recalledPearl Milling | Cereles En General Sas | Undeclared Allergens | PR |
| Food | CLASS I | Mint Leaf Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS I | Zapp's Big Cheezy Potato Chips recalled by Utz Quality FoodsZapp's Big | Utz Quality Foods | Salmonella | 34 states |
| Food | CLASS I | Coffee Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS I | Earl Grey Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS II | El David Gelee, Bonbons with fruits Soft & Juicy recalledEl David | Alb-USA Enterprises | Undeclared Allergens | NJ, NY |
| Food | CLASS II | Joy Strawberry Lassi recalled by Joy Gourmet FoodsJoy | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Mixed Berry Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS II | Joy Mango Lassi recalled by Joy Gourmet FoodsJoy | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Lavender Rose Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS I | Sea Salt Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS II | Joy Masala Chaash Lassi recalled by Joy Gourmet FoodsJoy Masala | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS II | Joy Mango-Pina-Orange Lassi recalled by Joy Gourmet FoodsJoy Mango-Pina-Orange | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS II | Joy Mango-Pina-Strawberry Lassi recalled by Joy Gourmet FoodsJoy Mango-Pina-Strawberry | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Dirty Maui Onion Chip recalled by Utz Quality FoodsDirty Maui | Utz Quality Foods | Salmonella | 34 states |
| Food | CLASS II | Joy Sweet Lassi recalled by Joy Gourmet FoodsJoy | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS III | Roast beef and cheddar closed face sandwich recalledRoast | Produce Innovations | Packaging Defects | 4 states |
| Food | CLASS I | 25# Sunflower Seeds C/S recalled by George J Howe Company | George J Howe Company | Undeclared Tree Nuts | 25 states |
| Food | CLASS II | Joy Rose Lassi recalled by Joy Gourmet FoodsJoy Rose | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS II | Joy Plain Chaash Lassi recalled by Joy Gourmet FoodsJoy Plain | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS I | Mulberry Fennel Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS I | No Salt Sunflower Seeds recalled by George J Howe CompanyNo Salt | George J Howe Company | Undeclared Tree Nuts | 25 states |
| Food | CLASS I | Mango Chili Date-Sweetened Chocolate recalled by Spring & Mulberry | Spring & Mulberry | Salmonella | Nationwide |
| Food | CLASS II | Joy Saffron Cardamon Lassi recalled by Joy Gourmet FoodsJoy Saffron | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |
| Food | CLASS II | Motor City Pizza Co. 5 Cheese Bread Single recalled by Champion FoodsMotor City | Champion Foods | Salmonella | Nationwide |
| Food | CLASS I | Zapp's Bayou Blackened Ranch Kettle Chips recalled by Utz Quality FoodsZapp's Bayou | Utz Quality Foods | Salmonella | 34 states |
| Food | CLASS I | Dirty Sour Cream and Onion Potato Chips recalled by Utz Quality FoodsDirty Sour | Utz Quality Foods | Salmonella | 34 states |
| Food | CLASS II | boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels recalled | Boichik Bagels | Undeclared Allergens | CA |
| Food | CLASS I | Dirty Brand Salt and Vinegar Potato Chips recalled by Utz Quality FoodsDirty | Utz Quality Foods | Salmonella | 34 states |
| Food | CLASS I | Dried Herring Fish recalled by Prime Food Processing | Prime Food Processing | Botulism | 19 states |
| Food | CLASS II | Joy Pineapple Lassi recalled by Joy Gourmet FoodsJoy | Joy Gourmet Foods | Processing Deviation | NJ, NY, PA |