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

2326–2350 of 6099

SevereFDA (Food)·F-0614-2024·2023-12-13
Fruit Combo Trays Recalled for Possible Salmonella Contamination
Market Cuts fruit combo trays (40 oz and 80 oz) are recalled due to possible salmonella contamination. Affected products were distributed in Illinois, Indiana, Michigan, and Wisconsin between November 4–9, 2023.
Product
Market Cuts 40 oz Combo Tray Fruit Small 40 Ounce tray UPC 092538001611; (No brand) 80 oz Combo Tray Fruit Large 80 Ounce tray UPC 092538001604; (No brand) 40 oz Combo Tray Fruit Small 40 Ounce tray UPC 092538001611; Market Cuts 80 oz Combo Tray Fruit Large 80 Ounce tray UPC 0925
Category
Food
Distribution
4 states
SevereCPSC·24727·2023-12-07
2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles Fire Hazard Recall
Segway Powersports is recalling about 1,100 2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles because the ignition coil can fail, allowing fuel to enter the exhaust pipe and ignite, creating a fire hazard. One vehicle fire with property damage has been reported.
Product
2022 Fugleman UT10E and UT10X Utility-Terrain Vehicles
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V822000·2023-12-07
Dutchmen Coleman Travel Trailers Recalled for Underrated Suspension Springs
Keystone RV is recalling 2021-2022 Dutchmen Coleman travel trailers with suspension springs rated at 4400 pounds instead of 5100 pounds. The underrated springs can become overloaded, increasing crash risk.
Product
DUTCHMEN — 2021 DUTCHMEN COLEMAN
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·24048·2023-12-07
XpressGoods recalls magnetic balls for federal toy safety violations
XpressGoods is recalling colorful neodymium magnetic balls that exceed federal safety limits for toy magnets. When swallowed, the magnets can lodge in the digestive system and cause serious injury or death.
Product
Colorful Metal Neodymium Magic Magnetic Balls - 8 color, 5mm
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0472-2024·2023-12-06
Le Croissant Chicken Salad recalled for undeclared milk and soy allergens
Le Croissant Chicken Salad (5.8 oz, sold as Jack & Olive, Sprig & Sprout, or Food Unlimited) has been recalled due to undeclared milk and soy allergens. Approximately 4,146 units were distributed across 15 states and Washington D.C.
Product
Le Croissant Chicken Salad Net Wt. 5.8oz (164g) UPCs:766375795018, 766375797128, 766375261599, 766375261599 Packaged in clamshell container. Sold under 3 brands: Jack & Olive, Sprig & Sprout, and Food Unlimited. Sold as single unit and 6-unit pack
Category
Food
Distribution
0 states
SevereFDA (Food)·F-0476-2024·2023-12-06
Eltahan Golden Raisins 400g recalled for undeclared sulfites
Eltahan Inc. is recalling Eltahan Golden Raisins (400g, UPC 2337660022) distributed in NY, NJ, and PA due to undeclared sulfites, which can cause severe allergic reactions.
Product
Eltahan Golden Raisins 400 gm. Packaged in a clear plastic bag. UPC 2337660022
Category
Food
Distribution
3 states
SevereFDA (Drugs)·D-0224-2024·2023-12-06
FDA recalls Artri King tablets for undeclared diclofenac
Botanical Be is recalling 235 bottles of Artri King tablets sold nationwide. The tablets contain undeclared diclofenac and were marketed without FDA drug approval.
Product
Artri King Reforzado con Origa y Omega 3 tablets, packaged in 100-count bottles, Manufactured by: Plantas medicinales de Mexico, Melchol Ocampo # 65 Local D, Delegacion Xochimilco CP 16800, Mexico DF, UPC 7 501031 111138
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0225-2024·2023-12-06
Reumo Flex caplets recalled for undeclared diclofenac content nationwide
Reumo Flex caplets packaged in 30-count boxes are being recalled because they contain undeclared diclofenac and were marketed without FDA approval. The product was distributed nationwide.
Product
Reumo Flex caplets, packaged in 30-count boxes, Manufactured by: Grupo Yepenza de Mexico, SA de CV, Comerciantes 5824 Col Arcos de Guadalupe, Zapopan Jal Mexico, UPC 7 502214 014598
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0473-2024·2023-12-06
Tuna Salad Recalled for Undeclared Milk and Soy Allergens
Le Croissant Tuna Salad (5.8oz) is recalled due to undeclared milk and soy allergens. Consumers with allergies to these allergens should not consume the product.
Product
Le Croissant Tuna Salad Net Wt. 5.8oz (164g) UPC:766375261605 Packaged in clamshell container. Sold under Food Unlimited brand. Sold as single unit and 6-unit pack
Category
Food
Distribution
0 states
SevereNHTSA·23V821000·2023-12-06
2023 BMW models recalled for transmission control unit weld defect
BMW is recalling certain 2023 models with a transmission control unit weld defect that may allow oil leakage, risking sudden power loss and increased crash risk.
Product
BMW — 2023 BMW 8 SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0226-2024·2023-12-06
Kuka Flex Forte caplets recalled for undeclared diclofenac and lack of FDA approval
Botanical Be is recalling Kuka Flex Forte caplets nationwide because they contain undeclared diclofenac and were marketed without required FDA approval. All lots expire 12/12/2024.
Product
Kuka Flex Forte caplets, packaged in 30-count bottles, Manufactured by: Kukamonga, Gonzalez Ortega No 170 Col Centro, 44100 Guadalajara Jal, UPC 0736640810265
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0145-2024·2023-12-06
Prescription drug oral solution recalled for microbial contamination
Bayer Healthcare Pharmaceuticals Inc. is recalling 192 bottles of VITRAKVI (larotrectinib) oral solution due to microbial contamination identified as Penicillium brevicompactum during routine testing.
Product
VITRAKVI — VITRAKVI (LAROTRECTINIB)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0480-2024·2023-12-06
GreenGate Fresh Spinach Recalled for Potential E. coli Contamination
GreenGate Fresh Cello Spinach is being recalled due to potential E. coli (EHEC) contamination. The recall involves 11 cases distributed to eight consignees across seven U.S. states.
Product
GreenGate Fresh Standard Cello Spinach; 4 - 2.5lb plastic bags per box; SKU 465; Perishable hence require refrigeration at all times of its shelflife
Category
Food
Distribution
7 states
CriticalCPSC·24719·2023-11-30
Peg Perego Inclined Sleeper Bassinets Recalled for Suffocation and Fall Risk
Peg Perego has recalled YPSI and Z4 inclined sleeper bassinets because they violate federal safety standards for infant sleep products and pose a risk of suffocation and falls.
Product
YPSI and Z4 Inclined Sleeper Bassinets
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·24722·2023-11-30
Polaris Model Year 2022 Patriot 850 MATRYX Snowmobiles Recalled for Injury Hazard
Polaris is recalling about 2,900 Model Year 2022 Patriot 850 MATRYX snowmobiles because the ring gear on the primary clutch can fail, causing clutch components to come loose and creating an injury hazard. Nine failures have been reported, including one injury.
Product
Polaris Snowmobiles, Model Year 2022 PATRIOT 850 MATRYX RMK, INDY and SWITCHBACK
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-0234-2024·2023-11-29
VariSoft Insulin Infusion Set Recalled Over Premature Connector Disconnection
Unomedical recalls 3,362 units of VariSoft infusion sets due to connector damage causing premature disconnection and missed insulin doses, risking dangerous elevation of blood glucose and ketone levels.
Product
VariSoft infusion set, Model Number 1002830
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0131-2024·2023-11-29
Eye Drops Recalled for Non-Sterility Issues from Manufacturing Facility
Cardinal Health is recalling LEADER brand Eye Irritation Relief drops due to non-sterility concerns. FDA testing found insanitary conditions and positive bacterial results at the manufacturing facility, affecting 11,629 units distributed nationwide.
Product
EYES IRRITATION RELIEF — EYES IRRITATION RELIEF (POLYVINYL ALCOHOL AND POVIDONE AND TETRAHYDROZOLINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0132-2024·2023-11-29
FDA Recalls Non-Sterile Dry Eye Relief Drops Due to Bacterial Contamination
Cardinal Health is recalling all lots of LEADER brand Dry Eye Relief nationwide due to non-sterility. FDA found insanitary manufacturing conditions and positive bacterial test results.
Product
DRY EYE RELIEF — DRY EYE RELIEF (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-0107-2024·2023-11-29
Polyvinyl Alcohol Eye Drops Recalled for Non-Sterile Manufacturing Conditions
FDA recalls Polyvinyl Alcohol 1.4% Lubricating Eye Drops nationwide due to non-sterile manufacturing conditions found during inspection.
Product
Polyvinyl Alcohol 1.4% Lubricating Eye Drops, packaged in 0.5 FL OZ (15mL) bottles, Dist. by: RUGBY LABORATORIES, Livonia, MI 48152, NDC 0536-1325-94.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0116-2024·2023-11-29
FDA Recalls Sodium Bicarbonate Injection for Silicone Particulate Contamination
Exela Pharma Sciences recalls 8.4% sodium bicarbonate injection nationwide due to silicone particulate matter in vials. The FDA classified this Class I recall as affecting 355,220 vials.
Product
SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0135-2024·2023-11-29
Eye drops recalled for non-sterility due to bacterial contamination
Cardinal Health's LEADER brand Dry Eye Relief eye drops are recalled nationwide due to non-sterility concerns. FDA found insanitary conditions and positive bacterial results from environmental sampling at the manufacturing facility.
Product
DRY EYE RELIEF — DRY EYE RELIEF (POLYETHYLENE GLYCOL AND PROPYLENE GLYCOL)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0233-2024·2023-11-29
VariSoft Infusion Set Model 1002828 Recalled for Connector Detachment Risk
The FDA recalls 1,679 VariSoft infusion sets (Model 1002828) due to connector damage that causes improper detachment. Undetected disconnections can lead to missed insulin doses and diabetic ketoacidosis.
Product
VariSoft infusion set, Model Number 1002828
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0108-2024·2023-11-29
Lubricating Tears Eye Drops Recalled for Non-Sterility and Bacterial Contamination
Rugby Laboratories' Lubricating Tears Eye Drops are being recalled nationwide due to non-sterility. FDA found insanitary conditions and positive bacterial test results at the manufacturing facility.
Product
Lubricating Tears Eye Drops (Dextran/Hypromellose), 0.1%/0.3%, packaged in 0.5 FL OZ (15mL) bottles, Distributed by: RUGBY LABORATORIES, Livonia, MI 48152, NDC 0536-1282-94
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0133-2024·2023-11-29
LEADER Lubricant Eye Drops Recalled Nationwide for Non-Sterility Concerns
LEADER brand Lubricant Eye Drops are being recalled nationwide due to non-sterility issues. FDA testing found insanitary conditions and positive bacterial contamination at the manufacturing facility.
Product
LUBRICANT DROPS — LUBRICANT DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0134-2024·2023-11-29
FDA Recalls LEADER Brand Lubricant Eye Drops Due to Non-Sterility Risk
Cardinal Health is recalling all lots of LEADER brand Lubricant Eye Drops nationwide due to non-sterility. FDA found insanitary conditions and positive bacterial test results from the manufacturing facility.
Product
LUBRICANT DROPS — LUBRICANT DROPS (CARBOXYMETHYLCELLULOSE SODIUM)
Category
Drug
Distribution
Distributed nationwide

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2326–2350 of 6099