Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

176–200 of 778

SevereFDA (Drugs)·D-0553-2026·2026-05-27
MG217 Multi-Symptom Treatment Cream recalled for microbial contamination
Wisconsin Pharmacal Company is recalling MG217 Multi-Symptom Treatment Cream & Skin Protectant due to confirmed presence of Staphylococcus aureus contamination. Affected units are 6 oz tubes with Lot #1024088, expiring 11/30/2026, distributed nationwide and in the Bahamas.
Product
MG217 Multi-Symptom Treatment Cream & Skin Protectant (colloidal oatmeal 2%), NET WT 6 oz (170 g), Manufactured by: Pharmacal 1 Pharmacal Way, P.O. Box 198, Jackson, WI 53037.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-0793-2026·2026-05-27
Flat Belly Bully beverage under-processing and unlawful health claims
LIQUID BLENZ CORP is recalling Flat Belly Bully 16 oz and 32 oz beverages due to potential under-processing that could allow Clostridium botulinum growth, and unlawful health claims on labeling.
Product
Flat Belly Bully 16 oz and 32 oz
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0544-2026·2026-05-27
Erythromycin Tablets Recalled for Impurity Above Acceptable Limits
Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.
Product
ERYTHROMYCIN — ERYTHROMYCIN (ERYTHROMYCIN)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2202-2026·2026-05-27
Swan-Ganz Catheters Models 131F7 Through AIQSGF8 Recalled Nationwide
Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.
Product
Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7, 831F75/831F75P, TS105F5, 774F75, 777F8, AIQSGF8;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0835-2026·2026-05-27
Good & Gather Mexican Street Corn Trail Mix Recalled for Potential Salmonella
John B Sanfilippo & Sons Inc is recalling Good & Gather Mexican Street Corn Trail Mix 8 oz bags due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Product
Good & Gather Mexican Street Corn Trail Mix 8 oz bag UPC 085239270240, 8 bags per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2227-2026·2026-05-27
Azurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage
The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.
Product
Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063), Azurion 3 M15 (722064), Azurion 7 B12 (722067), Azurion 7 B20 (722068), Azurion 7 M12 (722078), Azurion 7 M20 (722079, 722224).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2204-2026·2026-05-27
Swan-Ganz Pacing Catheter Model D200F7 Recall Due to Leak Risk
Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.
Product
Swan-Ganz Pacing Catheter, Models: D200F7;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2209-2026·2026-05-27
Tangent Single Use Digital Catheter Recalled for Distal Shaft Fractures
Tangent Endoscopy is recalling its Tangent Single Use Digital Catheter (models TNG4002-IND and TNG-4007-6pk) due to fractures observed at the distal shaft tip without complete detachment, posing a risk during endoscopic procedures.
Product
Tangent Endoscopy, Tangent Single Use Digital Catheter. Model Numbers: (1) TNG4002-IND. (2) TNG-4007-6pk.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2220-2026·2026-05-27
Medtronic DLP Retrograde Cannula 13FR Model 94913L Recall
Medtronic is recalling certain lots of DLP Retrograde Cannula (Model 94913L), a cardiopulmonary bypass catheter, due to potential sterile barrier breaches. The affected device was distributed worldwide.
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913L; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0831-2026·2026-05-27
Southern Style Nuts Gourmet Hunter Mix Recalled for Salmonella Risk
John B Sanfilippo & Sons Inc is recalling Southern Style Nuts Gourmet Hunter Mix due to potential Salmonella contamination. The recall affects 23 oz and 36 oz jars distributed nationwide.
Product
Southern Style Nuts Gourmet Hunter Mix 23 oz plastic jar UPC 085839073319 and 36 oz plastic jar UPC 085839071483. 23 oz 6 jars per case case and 96 jars per display. 36 oz 6 jars per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2219-2026·2026-05-27
Medtronic DLP Retrograde Cannula Cardiopulmonary Bypass Catheter Recall
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94913), a cardiopulmonary bypass vascular catheter, due to a potential sterile barrier breach.
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94913; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2225-2026·2026-05-27
Philips Azurion X-Ray Systems Table Movement Control Defect Recall
Philips Azurion X-ray imaging systems may experience impaired table movement due to mechanical wear in the Float Tabletop control. The control module defect could affect longitudinal and transverse table positioning during medical procedures.
Product
Philips Azurion systems not configured with an optional auxiliary pan handle. Includes the below product descriptions and corresponding model numbers. 1. Azurion 3 M12; Model Numbers: 722063, 722229. 2. Azurion 3 M15; Model Numbers: 722222, 722064, 722280, 722230. 3.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2229-2026·2026-05-27
Integris-Allura X-ray systems with degraded deaeration hoses recalled
Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.
Product
Integris-Allura system; System Code Description (Model Numbers): Integris CV Cesar-Powerpack-Visub-Nicol (722030), Integris Allura 15 & 12 (monoplane) (722043), INTEGRIS Allura 15-12 (biplane) (722044), Integris-Allura 9 (722018), Integris-Allura 9 (Biplane) (722021), Integris CV
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2217-2026·2026-05-27
Medtronic DLP Retrograde Cannula 15FR Model 94665 Sterile Barrier
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula Model 94665 due to potential sterile barrier breach. The product is used in cardiopulmonary bypass procedures worldwide.
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94665; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0836-2026·2026-05-27
Fisher Tex Mex Trail Mix Recalled for Potential Salmonella Contamination
Fisher Tex Mex Trail Mix 30 oz jars are recalled nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Product
Fisher Tex Mex Trail Mix 30 oz plastic jar UPC 070690275941, 6 jars per case
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0541-2026·2026-05-27
Liraglutide Injection Recalled Due to Particulate Matter in Cartridges
Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.
Product
LIRAGLUTIDE — LIRAGLUTIDE (LIRAGLUTIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2215-2026·2026-05-27
Medtronic GUNDRY Retrograde Cannula vascular catheter sterile barrier breach
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94115T) cardiopulmonary bypass vascular catheters due to potential sterile barrier breach. The affected product has been distributed worldwide.
Product
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94115T; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0820-2026·2026-05-27
Solina Sourdough Cheese Crouton Seasoning recalled for Salmonella contamination
Solina U.S. Holding is recalling Solina 6035415 Sourdough Cheese Crouton Seasoning (50 lb bags, Lot 355048) because it has the potential to be contaminated with Salmonella.
Product
Solina 6035415 Sourdough Cheese Crouton Seasoning, 50lb bag
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2203-2026·2026-05-27
Swan-Ganz Jr Catheter models recalled due to lumen hub leakage
Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.
Product
Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2214-2026·2026-05-27
Medtronic GUNDRY Retrograde Cannula Model 94113T sterile barrier recall
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.
Product
Medtronic GUNDRY Retrograde Cannula Manual-Inflate Silicone Body 13FR, Model 94113T; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2221-2026·2026-05-27
Medtronic DLP Retrograde Cannula cardiopulmonary bypass catheter
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.
Product
Medtronic DLP Retrograde Cannula Manual-Inflate Silicone Body 15FR, Model 94915; Cardiopulmonary bypass vascular catheter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0803-2026·2026-05-27
Liposomal Women's Liquid Multivitamin Drops Recalled for Manufacturing Deviations
Wellnov Supplements LLC is recalling Liposomal Women's Liquid Multivitamin Drops - Iron Free due to deviations from good manufacturing practices that could lead to bacterial pathogen and possible Clostridium botulinum contamination.
Product
Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid. Packaging: Aluminum bottle. 90 ml. Firm Address: Vitaminally LLC Chandler, AZ 85225.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2210-2026·2026-05-27
Oncology Kit With Extension Sets May Leak During Infusion Therapy
ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.
Product
Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros; ChemoLock; Syringe Transfer Set w/MicroClave, ChemoLock Port, REF: CL3960
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0549-2026·2026-05-27
Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid
Safecor Health is recalling a vitamin and mineral dietary supplement oral liquid due to the presence of black particles in the liquid. Affected lots were distributed in Ohio.
Product
Vitamin B-Complex, Vitamin C & Folic Acid Dietary Supplement Oral Liquid, Contains: Folic Acid 799 mcg/5mL, Delivers 5 mL per oral syringe, (Nephronex), Mfg By: LLORENS; Pkg by: Safecor, Columbus, OH. NDC 54859-0516-08
Category
Drug
Distribution
1 state
ModerateFDA (Devices)·Z-2213-2026·2026-05-27
OneLIF Interbody Cage Inserter Attachment Failure Recall
Novapproach Spine is recalling OneLIF Interbody Cages because the straight inserter may fail to properly attach to the cages, potentially causing procedural delays or the need to use an alternative implant.
Product
OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X 7mm - Oblique, 010-107-1209/Small 7 Degree 12mm X 9mm, 010-107-1411/Small 7 Degree 14mm X 11mm, 010-107-1613/Small 7 Degree 16mm X 13mm, 010-113-1006/Small,
Category
Medical Device
Distribution
Distributed nationwide

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