Recalls in April 2026 (page 4)
673 recalls.
- Blackstone Parmesan Ranch Seasoning recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - 1P Jalapeno Heat Unit for 300 lbs of Meat recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - 1P Original Smokehouse Unit for 300 lbs. of Meat recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - Ellsworth Sour Cream + Onion Seasoning recall (PS Seasoning & Spices, Inc.)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - C7139D1 Natural Parmesan Cheese Flavor recall (Fontana Flavors, Inc)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - VG7274D1 Natural Cream of Mushroom Type Flavor recall (Fontana Flavors, Inc)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - C0017D Natural & Artificial White Cheddar Cheese Flavor recall (Fontana Flavors, Inc)
FoodClass IReported May 27, 2026 · Product was made with milk powder recalled by the supplier due to Salmonella contamination. - MA Cohen's Kippered Herring vacuum packed recall (Shining Sea Fish Co. LLC)
FoodClass IReported May 27, 2026 · Clostridium botulinum is an uncontrolled hazard - Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging:... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging:... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - FulviLife Complex. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Joint Nourish. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns. - Liquid Blenz Good Brain Tonic 16 oz and 32 oz recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Flat Belly Bully 16 oz and 32 oz recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Blood Pressure Bully 16 oz and 32 oz recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Pure Shilajit Tonic 16 oz and 32 oz recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Prostate Bully 16 oz and 32 oz recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Fibroid Bully 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Menopause Bully 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Immunity Enhancer Elderberry 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Pure Libido Drink 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Pure Diabetes Bully 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Sea Moss Tonic 16 oz and 32. oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Blackseed Bitters 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - Liquid Blenz Soursop Bitters 16 oz and 32 oz. recall (LIQUID BLENZ CORP)
FoodClass IIReported May 27, 2026 · May be under-processed resulting in growth of Clostridium botulinum and lists health claims. - MG217 Multi-Symptom Treatment Cream & Skin Protectant recall (Wisconsin Pharmacal Company)
DrugClass IReported May 27, 2026 · Microbial Contamination of Non-Sterile Products: confirmed presence of Staphylococcus Aureus. - Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported May 27, 2026 · CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit - Erythromycin Tablets recall (Zydus Pharmaceuticals (USA) Inc)
DrugClass IIReported May 27, 2026 · CGMP Deviations; presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit - Liraglutide Injection recall (Lupin Pharmaceuticals Inc.)
DrugClass IIReported May 27, 2026 · Presence of particulate matter: a white thread-like structure in the cartridge - Atomoxetine Capsules HCL recall (Safecor Health, LLC)
DrugClass IIReported May 27, 2026 · Labeling: Label Mix-Up: Atomoxetine HCl 25mg Capsule incorrectly labeled as Atomoxetine HCl 10mg Capsule. - Primidone Tablets recall (Golden State Medical Supply Inc.)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Primidone Tablets recall (Golden State Medical Supply Inc.)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Primidone Tablets USP recall (Lannett Company Inc.)
DrugClass IIIReported May 27, 2026 · Cross contamination with other products: API contaminated with trace amounts of Acemetacin API. - Integris-Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in... - Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in... - Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · The deaeration hose in X-ray tube cooling units type CU3101, manufactured between February 2016 and May 2020, may degrade over time, potentially resulting in... - Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 ... recall (C.R. Bard Inc)
Medical deviceClass IIReported May 27, 2026 · Due to stain present on the surface of affected foley catheters. - Philips Azurion systems not configured with an optional auxiliary pan handle. Includes... recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported May 27, 2026 · Potential safety issue with Philips Azurion systems, where longitudinal and transverse table movements may be impacted due to mechanical wear of the Float... - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported May 27, 2026 · Certain lots of product have the potential for a sterile barrier breach. - OneLIF Interbody Cage recall (Novapproach Spine, LLC)
Medical deviceClass IIReported May 27, 2026 · Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the... - Swan-Ganz Pacing Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Swan-Ganz Jr Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Swan-Ganz Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Pure Ground Ingredients-Organic Peppermint Leaf Powder. wholesale bulk recall (Pure Ground Ingredients, Inc.)
FoodClass IReported May 20, 2026 · Product has the potential to be contaminated with Salmonella. - Kroger HOMESTYLE Cheese AND Garlic CROUTONS recall (Sugar Foods LLC)
FoodClass IReported May 20, 2026 · Possible Salmonella in croutons. The firm was notified by their supplier that the non-fat milk powder used to manufacture the product was recalled due to... - Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn recall (Prospector Popcorn, LLC)
FoodClass IIReported May 20, 2026 · Products contain undeclared soy, specifically soy lecithin. - Swad Mango Flavored Masala Candy recall (Raja Foods and Vegetables Inc.)
FoodClass IIReported May 20, 2026 · Contains undeclared Blue 1 - Swad Orange Flavored Masala Candy recall (Raja Foods and Vegetables Inc.)
FoodClass IIReported May 20, 2026 · Contains undeclared FD&C Yellow 6 - Uncle Giuseppe's Marketplace Milk Chocolate Bridge Mix recall (WE R NUTS)
FoodClass IIReported May 20, 2026 · Contains undeclared allergens (cashews, milk, and soy). - Frederik's by meijer Vanilla Bourbon Trail Mix recall (Ferris Coffee and Nut Company, Inc.)
FoodClass IIReported May 20, 2026 · Undeclared allergens (wheat and soy). - Dakota Honey Company the Honey Flight. 4 Flavors of Spreadable Spun Honey Original -... recall (Dakota Honey Company)
FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic) - Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic) - Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic) - Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic) - Dakota Honey Company Spreadable Spun Honey recall (Dakota Honey Company)
FoodClass IIReported May 20, 2026 · Foreign object (stainless steel dust/flakes or shreds of plastic) - Ascend Laboratories recall (Ascend Laboratories, LLC)
DrugClass IIReported May 20, 2026 · Failed Dissolution Specifications - Oasis Tears PF recall (Oasis Medical, Inc.)
DrugClass IIReported May 20, 2026 · Lack of Assurance of Sterility: The recall is being initiated out of an abundance of caution following FDA observations noted during a recent inspection of... - Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application recall (Medtronic Neuromodulation)
Medical deviceClass IIReported May 20, 2026 · Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in... - LVIS Intraluminal Support Device recall (MICROVENTION INC.)
Medical deviceClass IIReported May 20, 2026 · Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is... - Medtronic Marinr Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable BDB recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - Daig Livewire Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - CS Uni-Directional w Auto ID recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - CS Uni-Directional w Auto ID recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BW Webster Duo-Decapolar recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD EP XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD EP XT Decapolar Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic XT Deca Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product - BARD Dynamic Tip Steerable recall (Stryker Sustainability Solutions)
Medical deviceClass IIReported May 20, 2026 · Incomplete seals on sterile product