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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6376–6400 of 7498

  • SevereFDA (Drugs)·D-0645-2022·2022-03-02

    RISE UP RED EDITION Capsules recalled for undeclared tadalafil

    RISE UP RED EDITION Capsules, 650 mg, have been recalled because they contain undeclared tadalafil, an ingredient found in FDA-approved male sexual enhancement products. The product is an unapproved drug and was distributed nationwide via Amazon Marketplace.

    Product
    RISE UP RED EDITION Capsules, 650 mg, 10-count blisters packaged in a carton, ASIN B08JCWG84D, barcode X002NI8PE1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0778-2022·2022-03-02

    Kroger American Blend Lettuce Recalled for Listeria Contamination Risk

    Dole Fresh Vegetables recalls Kroger American Blend lettuce due to Listeria found on harvest equipment. Affected products distributed across the US and Canada have best-by dates from December 22, 2021 to January 9, 2022.

    Product
    Kroger 12 oz American Blend UPC: 0-11110-91041-7 SKU: 3003
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0781-2022·2022-03-02

    Dole recalls Kroger 24 oz lettuce salad due to Listeria

    Dole Fresh Vegetables is recalling Kroger 24 oz Classic Garden lettuce salad because harvest equipment was found contaminated with Listeria monocytogenes. Consumers should not eat the affected product.

    Product
    Kroger 24 oz Classic Garden UPC: 0-11110-91037-0 SKU: 3009
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0786-2022·2022-03-02

    Dole Little Salad Bar Shredded Lettuce Recalled for Listeria monocytogenes

    Dole Fresh Vegetables is recalling Little Salad Bar 8 oz Shredded Lettuce because harvest equipment was found to contain Listeria monocytogenes. Affected products have best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Little Salad Bar 8 oz Shredded Lettuce UPC: 4099100087963 SKU: 3404
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0745-2022·2022-03-02

    Dole Garden Salad recalled for Listeria contamination in harvest equipment

    Dole 12oz Garden Salad / Salade Du Jardin is recalled due to Listeria monocytogenes contamination detected in harvest equipment used for raw iceberg lettuce. Affected products have code dates between December 23, 2021 and January 8, 2022.

    Product
    Dole 12oz Garden Salad / Salade Du Jardin UPC:0-71430-01135-5 SKU: 2673
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0775-2022·2022-03-02

    Dole 9.1 oz Peppercorn Ranch Salad Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc is recalling its 9.1 oz Peppercorn Ranch salad for Listeria monocytogenes contamination found in harvest equipment. Consumers should not consume affected packages.

    Product
    Dole 9.1 oz Peppercorn Ranch / Ranch et Poivre UPC: 0-71430-00098-4 SKU: 1011
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0776-2022·2022-03-02

    Dole Peppercorn Ranch Chopped Kit Recalled Due to Listeria in Harvest Equipment

    Dole Fresh Vegetables recalls 9.1 oz Peppercorn Ranch Chopped Kits due to Listeria monocytogenes found in harvest equipment. The affected products were distributed across Canada and the United States.

    Product
    Dole 9.1 oz Peppercorn Ranch Chopped Kit UPC: 0-71430-00093-9 SKU: 728
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0774-2022·2022-03-02

    Dole Shredded Lettuce Recalled Due to Listeria monocytogenes in Harvest Equipment

    Dole Fresh Vegetables Inc is recalling Dole Shredded Lettuce because harvest equipment was found to contain Listeria monocytogenes. This is an FDA Class I recall.

    Product
    Dole 16 oz Shredded Lettuce UPC: 0-71430-84616-2 SKU: 157 2029 Dole 8 oz Shredded Lettuce UPC: 0-71430-01065-5 SKU 2029
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0762-2022·2022-03-02

    Presidents Choice Ranch Kit recalled for potential Listeria contamination

    Dole Fresh Vegetables is recalling Presidents Choice 12.25oz Ranch Kit because Listeria monocytogenes was detected in harvest equipment used for the lettuce.

    Product
    Presidents Choice 12.25oz Ranch Kit / Le Choix du President Ranch Kit de Salade UPC: 0-60383-00493-4 SKU: 3614
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0764-2022·2022-03-02

    President's Choice Sesame Ginger Kit Recalled for Listeria Contamination Risk

    Dole Fresh Vegetables is recalling President's Choice 13oz Sesame Ginger Kit due to Listeria monocytogenes detected in harvest equipment. Approximately 578,243 cases distributed across Canada and the United States are affected.

    Product
    President's Choice 13oz Sesame Ginger Kit / Le Choix du President Sesame et Gingembre UPC:0-60383-02320-1 SKU: 3283
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0783-2022·2022-03-02

    Little Salad Bar Caesar Salad Kit Recalled for Listeria Contamination

    Dole Fresh Vegetables is recalling Little Salad Bar Caesar Salad Kit due to Listeria monocytogenes detected in harvest equipment used for raw iceberg lettuce. Approximately 578,243 cases were distributed to multiple US states and Canadian provinces.

    Product
    Little Salad Bar 10 oz Caesar Salad Kit UPC: 4099100 087000 SKU: 3214
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0753-2022·2022-03-02

    Dole Chopped Teriyaki Pineapple Kit Recalled for Listeria Contamination

    Dole Fresh Vegetables Inc is recalling its 9.8oz Chopped Teriyaki Pineapple Kit due to Listeria monocytogenes detected in harvest equipment used for raw iceberg lettuce. The product was distributed across multiple U.S. states and Canadian provinces.

    Product
    Dole 9.8oz Chopped Teriyaki Pineapple Kit UPC:0-71430-00100-4 SKU: 791
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0777-2022·2022-03-02

    Dole Teriyaki Pineapple Kit recalled for Listeria contamination

    Dole is recalling certain Teriyaki Pineapple Kits due to Listeria monocytogenes detected in harvest equipment. Affected products have codes beginning with W and best-by dates from December 22, 2021 through January 9, 2022.

    Product
    Dole 9.8 oz Chopped Teriyaki Pineapple Kit UPC: 0-71430-00100-4 SKU: 791 Dole 9.8 oz Chopped Teriyaki Pineapple Kit / Teriyaki A L'ananas UPC: ¿0-71430-00182-0 SKU 1014
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0743-2022·2022-03-02

    Dole Iceberg Lettuce Recalled Due to Listeria Contamination

    Dole 11oz Greener Selection iceberg lettuce is being recalled due to Listeria monocytogenes found in harvest equipment. Approximately 578,243 cases were distributed across multiple US states and Canadian provinces.

    Product
    Dole 11oz Greener Selection UPC: 0-71430-01008-2 SKU: 34
    Category
    Food
    Distribution
    37 states
  • SevereFDA (Food)·F-0788-2022·2022-03-02

    Dole Recalls Marketside Iceberg Salad Due to Listeria Contamination

    Dole Fresh Vegetables is recalling Marketside 12 oz Classic Iceberg Salad due to Listeria monocytogenes detected in harvest equipment. Consumers should not eat the affected product and should discard or return it.

    Product
    Marketside 12 oz Classic Iceberg Salad UPC: 6-81131-32894-4 SKU: 3107
    Category
    Food
    Distribution
    37 states
  • SevereNHTSA·22V118000·2022-03-02

    Freightliner M2 Brake Drum Defect May Cause Loss of Brake Function

    Daimler Trucks is recalling certain 2020-2022 Freightliner M2 trucks due to brake drum cracking that can cause brake failure and increase crash risk. All vehicles have been remedied.

    Product
    FREIGHTLINER — 2021 FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0771-2022·2022-03-02

    Dole Southwest Salad Kit Recalled Due to Listeria Contamination Risk

    Dole Fresh Vegetables Inc is recalling its 13 oz Southwest Salad Kits due to Listeria monocytogenes detected in harvest equipment. Consumers should not consume affected products with best-by dates December 22, 2021 through January 9, 2022.

    Product
    Dole 13 oz Southwest Salad Kit UPC: 0-71430-01701-2 SKU: 2776
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Drugs)·D-0648-2022·2022-02-23

    HCG 6,000iu Injection Recalled for Bacterial Contamination

    Revive Rx is recalling HCG 6,000iu injectable medication due to bacterial contamination (Paenibacillus lautus) identified in the product. The affected lot was distributed nationwide.

    Product
    HCG 6,000iu (lyo) Human Chorionic Gonadotropin Inj., For Sub-Q or IM Use Only, Not For IV Use, Vial, Rx Only, Compounded By: Revive Rx 3831 Golf Dr., Houston, TX 77018, NDC: 88888-1739-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0629-2022·2022-02-23

    Arrow-Trerotola Percutaneous Thrombolytic Device Set Tip Separation Recall

    Teleflex Medical Inc. is recalling Arrow-Trerotola PTD catheter sets due to reported tip separation during use. The device is used for mechanical declotting of vascular access fistulae and grafts.

    Product
    Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), REF PT-65509 (finished good kit) The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native arterio-venous (AV) fist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0638-2022·2022-02-23

    RED MAMMOTH 400 mg Capsules Recalled for Undeclared Active Pharmaceutical Ingredients

    RED MAMMOTH capsules, 400 mg (Lot # DK1027, Exp. 08/01/2023) are being recalled because they contain undeclared sildenafil and tadalafil, making them an unapproved drug marketed without FDA authorization.

    Product
    RED MAMMOTH capsules, 400 mg, packaged in 10-count blisters per carton, ASIN B00KA8FBNI, barcode X001ANE0I5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0562-2022·2022-02-23

    MAC DADDY RED Capsules Recalled for Undeclared Drug Ingredients

    MAC DADDY RED Capsules are being recalled because they contain undeclared tadalafil and/or sildenafil without FDA approval. The product was distributed nationwide via Amazon Marketplace.

    Product
    MAC DADDY RED Capsules, packaged in 10-count blisters per carton, ASIN B07TLDZLY2, UPC 742137 605191.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0563-2022·2022-02-23

    MAC DADDY PURPLE Capsules Recalled for Undeclared Drug Ingredients

    ABC Sales 1 Inc is recalling MAC DADDY PURPLE Capsules because they contain undeclared tadalafil and/or sildenafil, active ingredients in FDA-approved prescription drugs, making the product an unapproved drug.

    Product
    MAC DADDY PURPLE Capsules, packaged in 10-count blisters per carton, ASIN B08Z63Z4QK, UPC 742137 605764.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0624-2022·2022-02-23

    Teleflex Arrow-Trerotola Percutaneous Thrombolytic Device PTD Kit recalled for tip separation

    Teleflex recalls approximately 1,400 Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) kits due to reports of tip separation during use. The medical device is used for dialysis graft declotting and has been distributed worldwide.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-65709-HFWC containing components: PT-65709-C, PT-03009, PT-65709-HFS The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0738-2022·2022-02-23

    Xuerong Brand Enoki Mushrooms Recalled for Listeria Contamination

    Golden Medal Mushroom Inc is recalling Xuerong brand enoki mushrooms because Listeria monocytogenes was detected in the product. The affected product was distributed in Illinois.

    Product
    Enoki Mushrooms, brand Xuerong, net wt. 200g/7.05-ounce packages, UPC 6 953150 100684. Product sent to distributor is packaged in a brown cardboard master case. The product name "ENOKI MUSHROOM" and other information in Chinese are printed in green color. The code "30051
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0633-2022·2022-02-23

    HYDROmorphone HCl syringe recalled due to labeling mix-up

    STAQ Pharma is recalling HYDROmorphone HCl PF syringes (lot 21104221A) that were incorrectly labeled as Morphine Sulfate PF. The mislabeling affects approximately 905 syringes distributed in Colorado, Ohio, and Texas.

    Product
    HYDROmorphone HCl PF 10 mg/50 mL (0.2mg/mL) in NaCl, 50 mL in 50 mL Single Dose Syringe, Rx only, STAQ Pharma, Inc., Denver, CO 80239, NDC: 73177-0104-05.
    Category
    Drug
    Distribution
    3 states