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.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

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

1501–1525 of 5642

SevereFDA (Food)·F-1018-2024·2024-03-06
Sargento Shredded Taco Cheese Blend Recalled for Listeria monocytogenes
Sargento Foods is recalling Sargento Deep V Shredded Taco Cheese Blend (UPC 46100352281) due to potential Listeria monocytogenes contamination. The recall affects 956 cases distributed across 15 states.
Product
Sargento Deep V Shredded Taco Cheese Blend Material #10002484, UPC 46100352281. Pack Size 500/.6 oz. Net Wt 18.750 lbs. Keep Refrigerated. Product of USA. Distributed By Sargento Foods Inc, Plymouth, WI 53073 USA.
Category
Food
Distribution
15 states
SevereFDA (Devices)·Z-1116-2024·2024-03-06
Medline Prep Kits Recalled Due to Non-Sterile Components
Medline is recalling 1,270 prep kits containing components that may lack sterility. Solutions from Nurse Assist used in the kits may not be sterile.
Product
Medline Kits, trays, and packs labeled as follows: a) C L PREP, REF DYNJ69664; b) DMEK PREP PACK, REF DYNJ81659A; c) PRE OP KIT 1, REF DYKS1377; d) PRE OP KIT 1, REF DYKS1377A
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1003-2024·2024-03-06
Rojo Black Bean 6 Layer Dip Recalled for Potential Listeria Contamination
Lakeview Farms LLC is recalling Rojo Black Bean 6 Layer Dip due to potential Listeria monocytogenes contamination. Consumers should not consume the product and should discard or return it.
Product
Rojo Black Bean 6 Layer Dip packaged in 20oz PET plastic containers, sold in sleeve with two containers per sleeve. 12 sleeves per case.
Category
Food
Distribution
0 states
SevereFDA (Devices)·Z-1164-2024·2024-03-06
Medtronic Duet External Drainage System catheter disconnection risk recalled
Medtronic recalls Duet External Drainage and Monitoring System catheter units (REF 46915) due to potential disconnection from stopcock connectors. Worldwide distribution includes 14,139 units.
Product
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Catheter, REF 46915, Sterile EO, Rx Only. Used to drain cerebrospinal fluid (CSF) as a means to reduce intracranial pressure and CSF volume.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1119-2024·2024-03-06
Medline Tracheostomy Care Kits and Trays Recalled Due to Sterility Concerns
Medline Industries is recalling tracheostomy care kits and trays due to potential lack of sterility in their component irrigation solutions. The non-sterile solutions pose a risk during patient care procedures.
Product
Medline Kits, trays, and packs labeled as follows: a) TRACH CARE KIT, REF DYND40589; b) TRACH CARE KIT, REF DYNDA3004; c) TRACHEOSTOMY CARE TRAY, REF DYND40650; d) TRAY,TRACH,W/PCLNR,14FR CATH N, REF DYND40594
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1099-2024·2024-03-06
Medline Centurion maintenance flush kits recalled for sterility failure
Medline Industries is recalling Centurion maintenance flush and blood draw kits that may lack sterility due to defective components, potentially allowing infections during medical procedures.
Product
Centurion Kits, trays, and packs labeled as follows: MAINTENANCE FLUSH KIT/BLOOD DRAW, REF DT19335A
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23V167000·2024-03-03
2023 Alliance RV Valor travel trailers recalled for incorrect wheel assemblies
Alliance RV is recalling certain 2023 Valor 21T15 travel trailers with incorrect wheel and tire assemblies that may become overloaded. Overloaded tires can fail and increase the risk of crashes.
Product
ALLIANCE RV — 2023 ALLIANCE RV VALOR
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24137·2024-02-29
Camplux Portable Tankless Water Heaters Recalled Due to Fire Hazard
About 42,000 Camplux portable tankless water heaters can leak gas from the regulator connection, creating a fire hazard. The Home Appliances is offering free repair kits with replacement regulators.
Product
Camplux portable tankless water heaters
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-1046-2024·2024-02-28
Dover Foley catheter kits recalled due to defective supplier components
Cardinal Health is recalling Dover brand Foley catheter kits due to components recalled by supplier Nurse Assist. Approximately 435,060 units were distributed to the US, Europe, Japan, and Latin America.
Product
Dover URINE METER ADD-A-FOLEY TRAY, 200 ML, NEEDLE SAMPLING PORT, DRAIN TUBE, PREP TRAY; Dover UNIVERSAL TRAY, 1000 ML BASIN, PVP SWAB STICKS, PREPPING COMPONENTS, 30 CC PRE-FILLED SYRINGE; Dover URINE DRAINAGE ADD-A-FOLEY TRAY, NEEDLE SAMPLING, A/R, DRAIN TUBE, PREP TRAY, 30 ML
Category
Medical Device
Distribution
0 states
CriticalFDA (Devices)·Z-1081-2024·2024-02-28
Surgical ocular pack kits recalled due to saline sterility assurance loss
Windstone Medical Packaging is recalling 80 Aligned Medical Solutions ocular pack surgical kits because sterility of the included saline cannot be guaranteed.
Product
Aligned Medical Solutions, In House Ocular Pack, AMS12947, STERILEEO
Category
Medical Device
Distribution
3 states
SevereFDA (Devices)·Z-1079-2024·2024-02-28
Surgical Kit with Saline Recalled Over Sterility Assurance Issue
Windstone Medical Packaging is recalling a surgical kit due to inability to guarantee sterility of the included saline. The recall affects 1,528 units distributed in Florida, Illinois, and California.
Product
Aligned Medical Solutions, Local Lower Extremity Pack I, AMS10833, STERILEEO
Category
Medical Device
Distribution
3 states
SevereFDA (Devices)·Z-1052-2024·2024-02-28
Dover Foley Catheter Kits and Drain Trays Recalled
Dover Foley catheter kits and silicone drain trays manufactured with subsequently recalled components were distributed to 924 units across the US, EMEA, Japan, and Latin America.
Product
Dover" 100% SILICONE FOLEY TRAY, NEEDLELESS, 14 FR (4.7 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" HYDROGEL COATED LATEX FOLEY CATHETER KIT, 5 CC, 2-WAY, 14 FR (4.7 MM), 10 CC WATER SYRINGE
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1001-2024·2024-02-28
Baxter Exactamix Pro 1200 Software Error Causes Medication Over-delivery
Baxter Healthcare is recalling the Baxter Exactamix Pro 1200 medication compounding device due to a software error that may cause ingredient over-delivery when using the 'Use Some Overfill' feature.
Product
Baxter Exactamix Pro 1200, REF EXM12DY
Category
Medical Device
Distribution
22 states
SevereFDA (Food)·F-0910-2024·2024-02-28
Ham and Cotija Torta Sandwiches Recalled for Listeria Contamination
Compass Group USA, Inc. is recalling 206 Ham & Cotija Torta Sandwiches due to Listeria monocytogenes contamination in Cotija cheese. Products were distributed in Florida with use-by dates of February 9-16, 2024.
Product
Ham & Cotija Torta Sandwich on Telera Roll, 8.3 oz, plastic container, UPC 100001002017
Category
Food
Distribution
0 states
SevereFDA (Drugs)·D-0346-2024·2024-02-28
TING Athlete's Foot Spray Recalled Due to Benzene Contamination
Insight Pharmaceuticals is recalling TING 1% Tolnaftate Athlete's Foot Spray due to benzene contamination. The recall affects approximately 59,644 cans distributed nationwide.
Product
TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1045-2024·2024-02-28
Dover Foley Catheter and Urinary Drainage Kits Recalled for Defective Components
Cardinal Health is recalling Dover foley catheter and urinary drainage kits containing components previously recalled by supplier Nurse Assist. The FDA Class I recall affects 17,640 units distributed to the US, EMEA, Japan, and Latin America.
Product
Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, NEEDLE PORT, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" HYDROGEL COATED LATEX 400 ML U/M FOLEY TRAY, NEEDLE, 16 FR (5.3 MM), 5 CC, 2000 ML BAG; Dover" UNIVERSAL TRAY, 1000 ML BASIN, PVP SOLUTION, PREPPING COMPONENTS, 10 ML PRE-FILL
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1080-2024·2024-02-28
Surgical ocular packs recalled for loss of saline sterility
Windstone Medical Packaging recalled 128 surgical eye kits because the included saline cannot be guaranteed sterile, risking post-operative infection.
Product
Aligned Medical Solutions, In House Ocular Pack, AMS12947A STERILEEO
Category
Medical Device
Distribution
3 states
SevereFDA (Devices)·Z-1049-2024·2024-02-28
Dover Irrigation Convenience Kits Recalled for Component Defects
Cardinal Health is recalling Dover Irrigation convenience kits that contained components which were separately recalled. The recall affects over 63,000 units distributed across the US, EMEA, Japan, and Latin America.
Product
Dover" IRRIGATION 1200 CC TRAY, 60 CC PISTON SYRINGE, STERILE SALINE, TIP PROTECTOR, ALCOHOL, LIDDED
Category
Medical Device
Distribution
0 states
SevereFDA (Drugs)·D-0333-2024·2024-02-28
FDA Recalls Neptune's Fix Tianeptine Elixir for Containing Unapproved Drug
Neptune's Fix Tianeptine Elixir has been recalled because it contains tianeptine, an unapproved drug substance in the United States. Approximately 1 million bottles distributed nationwide are affected.
Product
Neptune's Fix, Tianeptine Elixir, Fast Acting, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0334-2024·2024-02-28
Drug Recalled for Marketing Unapproved Tianeptine Without FDA Approval
Neptune's Fix Tianeptine Elixir is recalled nationwide for containing tianeptine, an FDA-unapproved substance. The product was marketed without required FDA approval.
Product
Neptune's Fix, Tianeptine Extra Strength Elixir, 0.338 fl oz (10 mL) bottle, Distributed By Neptune Resources, LLC, 30 N. Gould Street, Ste R, Sheridan, WY 82801.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0909-2024·2024-02-28
Hale and Hearty Tomato Basil and Rice Soup Recalled for Undeclared Soy
Hale and Hearty Soups is recalling Tomato Basil and Rice soup (UPC 635508547872) due to undeclared soy allergen. Consumers with soy allergies should not consume this product.
Product
Hale and Hearty Soups; Tomato Basil and Rice; UPC 635508547872
Category
Food
Distribution
1 state
SevereFDA (Drugs)·D-0343-2024·2024-02-28
Herbal dietary supplement recalled for undeclared drug ingredient
Sustain Herbal Dietary Supplement is being recalled nationwide for containing undeclared tadalafil, a pharmaceutical ingredient. The product was marketed as a dietary supplement but contains an unapproved drug.
Product
Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1050-2024·2024-02-28
Dover Foley Catheter Kits Recalled Due to Defective Components
Cardinal Health is recalling 4,620 Dover Foley catheter convenience kits due to components that were recalled by Nurse Assist. The kits, distributed in the US, EMEA, Japan, and Latin America, contain silicone and latex catheters.
Product
Dover" 100% SILICONE FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG, DRAIN SPOUT; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, LUER LOCK, 16 FR (5.3 MM), 5 CC, 2000 ML DRAIN BAG; Dover" 100% SILICONE 400 ML U/M FOLEY TRAY, COUD¿ TIP, 16 FR (5.3 MM), 5 CC, 2000 ML D
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-1043-2024·2024-02-28
Argyle Suction Catheter Trays with Chimney Valve recalled for defective components
Cardinal Health is recalling multiple Argyle Suction Catheter Tray models due to defective components. The kits containing these recalled components were distributed in the US, Europe, Japan, and Latin America.
Product
Argyle" Suction Catheter Tray with Chimney Valve Sterile Saline 18 Fr/Ch (6.0mm); Argyle" Suction Catheter Tray with Chimney Valve Sterile Saline, 6 Fr/Ch (2.0 mm); Argyle" Graduated Suction Catheter Tray with Chimney Valve Sterile Saline 8 Fr/Ch (2.67 mm); Argyle" Suction Cathet
Category
Medical Device
Distribution
0 states
SevereFDA (Drugs)·D-0345-2024·2024-02-28
Dietary supplement Arize recalled for undeclared pharmaceutical ingredient
Arize Herbal Dietary Supplement contains an undeclared ingredient (nortadalafil), a pharmaceutical used in FDA-approved male sexual enhancement medications, making it an unapproved drug.
Product
Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com
Category
Drug
Distribution
Distributed nationwide

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1501–1525 of 5642