The Recall Desk

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.

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Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

6851–6875 of 7514

  • SevereFDA (Food)·F-0170-2022·2021-11-24

    Whole Raw Red Onions from Mexico Recalled for Salmonella Risk

    Keeler Family Farms is recalling whole raw red onions imported from Chihuahua, Mexico due to potential contamination with Salmonella Oranienburg. The affected onions were shipped between July 1 and August 25, 2021, and distributed nationwide and to Ontario, Canada.

    Product
    Whole raw onions - RED - imported from Chihuahua, Mexico and shipped from July 1, 2021 through August 25, 2021. Products are packaged in 25 lb. and 50 lb. mesh bags. One pallet contains 42 bags. Store in cool dry place off the ground. Labeling will state product of Mexico on bill
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0248-2022·2021-11-24

    Lotrimin AF Powder Spray Recalled for Benzene Contamination

    Bayer Healthcare is recalling Lotrimin AF miconazole nitrate 2% powder spray due to the presence of benzene chemical contamination. The recall affects approximately 3.8 million cans distributed nationwide.

    Product
    LOTRIMIN AF, (Miconazole nitrate 2%), Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-0544-2 UPC 3 11017 41025 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0236-2022·2021-11-24

    LOTRIMIN AF Miconazole Nitrate Powder Spray Recalled for Benzene Contamination

    Bayer is recalling LOTRIMIN AF Deodorant Powder Spray due to potential benzene contamination from manufacturing deviations at a facility where other lots were found contaminated. The recall affects 2,817,468 cans distributed nationwide in the US, Puerto Rico, Canada, and Mexico.

    Product
    LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0184-2022·2021-11-24

    Green Giant Fresh Whole White Onions Recalled for Salmonella

    Green Giant Fresh brand whole white onions in 2 lb. bags are being recalled due to potential Salmonella Oranienburg contamination. The affected onions were distributed in Minnesota and North Dakota.

    Product
    Green Giant Fresh brand, Whole WHITE Onions packaged in 2 lb. flexible mesh bags, UPC 60580600218-2.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0249-2022·2021-11-24

    Lotrimin Daily Prevention Deo Tolnaftate Spray Recalled for Benzene Contamination

    Bayer Healthcare Pharmaceuticals is recalling Lotrimin Daily Prevention Deo (Tolnaftate 1%) spray powder due to the presence of benzene contamination. The recall affects 579,456 cans distributed nationwide.

    Product
    LOTRIMIN DAILY PREVENTION DEO — LOTRIMIN DAILY PREVENTION DEO (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0253-2022·2021-11-24

    Tinactin Tolnaftate Powder Spray Recalled Due to Benzene Contamination

    Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) Powder Spray because some cans contain benzene contamination. Consumers should stop using affected lots and consult a healthcare provider.

    Product
    Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can, labeled as (a) Product of Ireland 86940418; (b)Product of Finland 20006106; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 3 11017 41009 7, NDC 11523-0777-2.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0188-2022·2021-11-24

    Fisherman's Wharf Cooked Shrimp Recalled for Listeria Risk

    Fisherman's Wharf Shrimp 16/20 Cooked Shrimp 16oz packages are being recalled due to potential contamination with Listeria monocytogenes. The affected products were distributed domestically with specific serial numbers and best-by dates in early April 2023.

    Product
    Fisherman's Wharf, Shrimp 16 /20 Cooked Shrimp 16oz 7306067
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0247-2022·2021-11-24

    LOTRIMIN AF Miconazole Nitrate Powder Spray Recall for Benzene Contamination

    Bayer Healthcare Pharmaceuticals is recalling LOTRIMIN AF Jock Itch Powder Spray (4.6 oz, Miconazole Nitrate 2%) because certain lots contain benzene, a chemical contaminant.

    Product
    LOTRIMIN AF, (Miconazole nitrate 2%), Jock Itch, Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-4140-2. UPC 3 11017 41031 8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0207-2022·2021-11-24

    Dole Garden Salad Recalled for Listeria monocytogenes

    Dole Garden Salad (24 oz) has been recalled because Listeria monocytogenes was detected during testing by the Georgia Department of Agriculture. The affected lots were distributed across ten US states.

    Product
    Dole Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 24 oz. (1 lb. 8 oz.) 680 g UPC: 0 71430 01136 2 Dole Food Company, Inc. Distributed by Dole Fresh Vegetables, Monterey, CA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0173-2022·2021-11-24

    Red Onions Recalled for Potential Salmonella Contamination

    Sysco Merchandising and Supply is recalling 2,902 cases of red onions packed in 5-pound bags due to potential Salmonella contamination. The onions were distributed to multiple states.

    Product
    Red onions packed in 5 pound bag
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-0196-2022·2021-11-24

    HelloFresh Meal Kit Recalled for Salmonella Oranienburg Contamination

    HelloFresh has recalled meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. The affected products were produced in Week 35 (starting August 25, 2021) and distributed nationwide.

    Product
    HelloFresh Meal Kit Product Code 4-12-14-18-23-25-AA from Production Week 35 (production week start date: 8/25/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0234-2022·2021-11-24

    Arrow-Trerotola Percutaneous Thrombolytic Device: Inner Lumen Detachment Risk

    Arrow International is recalling 1918 units of the Arrow-Trerotola Percutaneous Thrombolytic Device due to inner lumen detachment that can cause embolization, requiring emergency retrieval and delaying treatment.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-WC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0206-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella-Contaminated Onions

    EveryPlate meal kits distributed nationwide are being recalled because they contain onions purchased from ProSource that are associated with a Salmonella Oranienburg outbreak.

    Product
    EveryPlate Meal Kit Product Codes 82-83-89-93-94-96-98 from Production Week 36 (production week start date: 09/01/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0185-2022·2021-11-24

    Red Onions Recalled for Potential Salmonella Contamination

    Hardies Fruit & Vegetable Co., LP is recalling red onions (Jumbo and Medium sizes) due to potential Salmonella contamination. Affected products were distributed in Texas.

    Product
    Onion Red Jumbo packed in a 5 pound cardboard box Product Code 2307, Onion Red Medium packed in a 5 pound cardboard box Product Code 2308
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0244-2022·2021-11-24

    Tinactin Jock Itch Powder Spray Recall Due to Benzene Contamination

    Bayer Healthcare is recalling 592,416 cans of Tinactin (Tolnaftate 1%) Jock Itch Powder Spray distributed nationwide due to potential benzene contamination. The product was manufactured at a facility where other lots were found to be contaminated with benzene.

    Product
    Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY NET WT133g (4.6 oz) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Ireland 86951967, UPC 3 11017 41007 3, NDC 11523-0072-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0209-2022·2021-11-24

    Kroger Garden Salad Recalled Due to Listeria Contamination

    Kroger Garden Salad has been recalled because the Georgia Department of Agriculture detected Listeria monocytogenes in the product. The recall affects specific lot codes distributed to multiple states.

    Product
    Kroger Garden Salad; iceberg lettuce, shredded carrots, red cabbage; Net Wt. 12 oz. (340g) UPC: 0-11110-91036-3 Distributed by The Kroger Company, Cincinnati, OH
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Drugs)·D-0246-2022·2021-11-24

    Lotrimin AF Deodorant Powder Spray Recalled for Benzene Contamination

    Bayer Healthcare is recalling Lotrimin AF Deodorant Powder Spray (Miconazole nitrate 2%) nationwide due to the presence of benzene contamination. The recall affects approximately 2.8 million cans distributed across the US, Puerto Rico, Canada, and Mexico.

    Product
    LOTRIMIN AF (Miconazole nitrate 2%) Deodorant Powder Spray, NET WT 133g (4.6 OZ) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Spain, NDC 11523-1272-2 UPC 3 11017 41023 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0252-2022·2021-11-24

    Tinactin Tolnaftate Jock Itch Powder Spray Recall Due to Benzene Contamination

    Bayer Healthcare is recalling Tinactin Tolnaftate 1% Jock Itch Powder Spray due to the presence of benzene contamination. The product was distributed nationwide in the US, Puerto Rico, Canada, and Mexico.

    Product
    Tinactin (Tolnaftate 1%) JOCK ITCH POWDER SPRAY NET WT133g (4.6 oz) can, Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland 20066104 UPC 3 11017 41007 3, NDC 11523-0072-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0232-2022·2021-11-24

    Arrow-Trerotola Percutaneous Thrombolytic Device Catheter Lumen Detachment Recall

    Arrow International is recalling Arrow-Trerotola Percutaneous Thrombolytic Device catheters because the inner lumen can detach from the device basket, causing embolization requiring additional intervention and delaying dialysis therapy. Approximately 1,245 units are affected worldwide.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-HFWC The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-veno
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V923000·2021-11-24

    2022 Ford Super Duty F-250 and F-350 Driver-Side Air Bag Cover Defect Recall

    Ford is recalling 2022 Super Duty F-250 and F-350 vehicles due to an insufficient driver-side air bag cover that may break apart during a crash, projecting fragments toward occupants and increasing injury risk.

    Product
    FORD — 2022 FORD F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0202-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination Risk

    EveryPlate meal kits from production week 08/04/2021 are being recalled because they contain onions contaminated with Salmonella Oranienburg. The onions were purchased from ProSource.

    Product
    EveryPlate Meal Kit Product Codes 81-82-84-90-92-95-98-99 from Production Week 32 (production week start date: 08/04/2021)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0233-2022·2021-11-24

    Arrow-Trerotola Percutaneous Thrombolytic Device inner lumen detachment and embolization risk

    Arrow-Trerotola PTD catheters are being recalled because the inner lumen can detach from the device basket, causing embolization that requires additional intervention. 1,167 units are affected.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit Percutaneous Thrombolytic Device : 7FR Product Code: PT-65709-W The Arrow-Trerotola" Percutaneous Thrombolytic Device (PTDTM) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venousf
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0174-2022·2021-11-24

    White Onions Recalled for Potential Salmonella Contamination

    Sysco Merchandising and Supply is recalling white onions packed in 10-pound bags due to potential Salmonella contamination. The affected product was distributed across 15 states.

    Product
    White onions packed in 10 pound bag
    Category
    Food
    Distribution
    15 states
  • SevereFDA (Food)·F-0180-2022·2021-11-24

    Red Jumbo Onions Recalled for Potential Salmonella Contamination

    JF Palmer & Sons Produce is recalling 1,040 bags of red jumbo onions due to potential Salmonella contamination. The affected onions were distributed to MN, TX, CA, and MD.

    Product
    Onions Red Jumbo, packaged in 25 pound bulk bags
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-0198-2022·2021-11-24

    EveryPlate Meal Kits Recalled for Salmonella Contamination Risk

    HELLOFRESH US is recalling specific EveryPlate meal kits from production week 07/07/2021 due to onions contaminated with Salmonella Oranienburg. The affected products were distributed nationwide.

    Product
    EveryPlate Meal Kit Product Codes 82-83-86-88-89-91-92-94-95-96-97-99-100 from Production Week 28 (production week start date: 07/07/2021)
    Category
    Food
    Distribution
    Distributed nationwide