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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8176–8200 of 36567

  • 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-0630-2022·2022-02-23

    THE RED PILL EXTRA STRENGTH Capsules Recalled for Undeclared Tadalafil

    THE RED PILL EXTRA STRENGTH 800 mg capsules are being recalled because they contain undeclared tadalafil, an active ingredient in FDA-approved sexual-enhancement medications. The product was marketed and distributed as an unapproved drug nationwide via Amazon.

    Product
    THE RED PILL, EXTRA STRENGTH capsules, 800 mg, packaged in 10-count blisters packaged in a carton, ASIN B0847BSQQ5, Barcode X002G5GMJ1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • 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
  • SevereFDA (Devices)·Z-0623-2022·2022-02-23

    Arrow-Trerotola Thrombolytic Device Tip Separation During Use Recalled

    Teleflex Medical is recalling Arrow-Trerotola PTD kits due to reports of tip separation during use. The affected device is used for declotting dialysis grafts and fistulae.

    Product
    Arrow-Trerotola Over-The-Wire PTD Kit, Percutaneous Thrombolytic Device, REF PT-12709-WC, containing components: PT-12709-CA, PT-12709-C, The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V100000·2022-02-22

    2021 Porsche Taycan: Center Seat Belt Buckle May Block Child Seat Anchors

    Porsche is recalling 2020-2021 Taycan vehicles with optional rear center seats. The center seat belt buckle wiring harness may obstruct access to child seat anchors, preventing proper installation.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V098000·2022-02-18

    Mercedes-Benz Recalls 2020 GLE 350 for Wiring Harness Defect

    Mercedes-Benz is recalling 2020 GLE 350 vehicles because an unsecured wiring harness may disable power steering, headlights, or wipers, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V096000·2022-02-18

    Kia Recalls 2014 Soul Vehicles Due to Air Bag Software Defect

    Kia is recalling 2014 Soul vehicles because the front air bags may not deploy in a crash if the control unit loses communication with sensors.

    Product
    KIA — KIA SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·006-2022·2022-02-18

    Corfu Foods Recalls Swai Fillets Imported Without Reinspection

    Corfu Foods is recalling 6,570 pounds of frozen swai fillets imported from Vietnam without required reinspection. No illnesses have been reported.

    Product
    Corfu Foods, Inc. Recalls Swai (Siluriformes) Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    4 states
  • SevereNHTSA·22V091000·2022-02-17

    2022 Chevrolet Corvette rear driveshaft defect may cause loss of power

    General Motors is recalling 2021-2022 Chevrolet Corvette vehicles whose rear half-shaft assemblies may be missing ball bearings. This can cause sudden loss of drive power, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET CORVETTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V093000·2022-02-17

    Kia Recalls 2013-2014 Optima Vehicles for Fuel Hose Fire Risk

    Kia is recalling 2013-2014 Optima vehicles previously repaired under recall 20V-100 because a damaged or missing heat-protective tape on the low-pressure fuel hose can cause a fuel leak and increase fire risk.

    Product
    KIA — KIA OPTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0694-2022·2022-02-16

    Kroger Organic Power Greens Recall Due to Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Kroger 5oz Organic Power Greens due to potential Listeria monocytogenes contamination. The recall affects approximately 2.3 million cases distributed across 43 states.

    Product
    Kroger 5oz Organic Power Greens Clamshell Product UPC 111110917331
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0712-2022·2022-02-16

    Marketside 6oz Baby Greens Recalled Due to Potential Listeria Monocytogenes

    Dole Fresh Vegetables Inc is recalling Marketside 6oz Baby Greens for potential Listeria monocytogenes contamination. Products were distributed across 36 states with Best if Used By dates from November 30, 2021 to January 8, 2022.

    Product
    Marketside 6oz Baby Greens Product UPC 681131355025
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0675-2022·2022-02-16

    Dole, Lidl, and Little Salad Bar chopped kits recalled for Listeria

    Dole, Lidl, and Little Salad Bar chopped salad kits are being recalled due to potential Listeria monocytogenes contamination. Products were distributed to 38 US states.

    Product
    Dole 13.6oz Sesame Asian Chopped Kit Product UPC 071430000359 Lidl 12oz Sesame Asian Chopped Kit Product UPC 4056489210450 Little Salad Bar 12oz Chopped Asian Kit Product UPC 4099100086973
    Category
    Food
    Distribution
    36 states
  • CriticalUSDA FSIS·005-2022·2022-02-16

    Morgan Foods Recalls Skyline Chili Cans for Undeclared Allergens

    Morgan Foods is recalling Skyline chili cans that contain undeclared milk, wheat, and soy allergens. The product may actually be cream of chicken soup.

    Product
    Morgan Foods, Inc. — Morgan Foods Recalls Skyline Chili Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0691-2022·2022-02-16

    Kroger Italian Blend Frozen Vegetables Recalled for Listeria Risk

    Dole Fresh Vegetables Inc is recalling Kroger 10oz Italian Blend vegetables (UPC 011110910455) due to potential Listeria monocytogenes contamination. Affected products with Best if Used By dates between November 30, 2021 and January 8, 2022 were distributed across 38 states.

    Product
    Kroger 10oz Italian Blend Product UPC 011110910455
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0656-2022·2022-02-16

    Dole Chopped Fiesta Lime Kit recalled for potential Listeria monocytogenes

    Dole Fresh Vegetables is recalling Chopped Fiesta Lime Kit (10.7oz) for potential Listeria monocytogenes. Affected products have lot codes beginning with N or Y and best-if-used-by dates from November 30, 2021 to January 8, 2022.

    Product
    Dole 10.7oz Chopped Fiesta Lime Kit Product UPC 071430000991
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0714-2022·2022-02-16

    Dole Organic Baby Romaine Clamshells Recalled for Potential Listeria Monocytogenes

    Dole Fresh Vegetables Inc is recalling two brands of 5oz organic baby romaine clamshells (Naturally Better and Nature's Promise) due to potential Listeria monocytogenes contamination. Products with specific date codes were distributed to 39 states.

    Product
    Naturally Better 5oz Organic Baby Romaine Clamshell Product UPC 607880203400 Nature's Promise 5oz Organic Baby Romaine Clamshell Product UPC 688267154485
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0705-2022·2022-02-16

    Marketside Cherry Almond Gorgonzola Chop Kit recalled for potential Listeria

    Dole Fresh Vegetables is recalling Marketside Cherry Almond Gorgonzola Chop Kit for potential Listeria monocytogenes. Affected products have codes N or Y with Best if Used By dates from November 30, 2021 to January 8, 2022.

    Product
    Marketside 13.8oz Cherry Almond Gorgonzola Chop Kit Product UPC 681131305167
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0711-2022·2022-02-16

    Spinach arugula blend recalled for potential Listeria monocytogenes

    Dole is recalling Marketside Organic Spinach Arugula Blend due to potential Listeria monocytogenes contamination affecting approximately 2.3 million cases.

    Product
    Marketside 5oz Organic Spinach Arugula Blend Clamshell Product UPC 681131532082
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0698-2022·2022-02-16

    Kroger Shredded Romaine Recalled for Potential Listeria Contamination

    Dole Fresh Vegetables Inc is recalling Kroger 8oz Shredded Romaine (UPC 011110221483) due to potential Listeria monocytogenes contamination. The product was distributed across 36 states.

    Product
    Kroger 8oz Shredded Romaine Product UPC 011110221483
    Category
    Food
    Distribution
    36 states
  • CriticalFDA (Food)·F-0692-2022·2022-02-16

    Kroger shredded green leaf recalled for potential Listeria contamination

    Kroger 4.5oz shredded green leaf products are recalled for potential Listeria monocytogenes. Affected items have codes starting with N or Y and best-if-used-by dates from November 30, 2021 to January 8, 2022.

    Product
    Kroger 4.5oz Shredded Green Leaf Product UPC 011110061065
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Drugs)·D-0561-2022·2022-02-16

    HARD DAWN Rise and Shine Capsules Recalled for Undisclosed Tadalafil

    HARD DAWN Rise and Shine capsules (500 mg) are being recalled because they contain tadalafil, an FDA-approved drug, without proper approval or labeling. The product was sold nationwide via Amazon.

    Product
    HARD DAWN, Rise and Shine capsules, 500 mg, packaged in 10-count blisters per carton, Made in Malaysia, UPC 680044 364926, ASIN: B077XCCL59
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0704-2022·2022-02-16

    Marketside Asian Chopped Kit Recalled for Potential Listeria

    Dole Fresh Vegetables is recalling Marketside 13.7oz Asian Chopped Kits due to potential Listeria monocytogenes contamination. Affected products should be discarded immediately.

    Product
    Marketside 13.7oz Asian Chopped Kit Product UPC 681131305150
    Category
    Food
    Distribution
    36 states
  • SevereFDA (Food)·F-0646-2022·2022-02-16

    Ahold Garden Salad Mix Recalled for Potential Listeria Monocytogenes

    Ahold 12oz Garden Salad Mix is recalled due to potential Listeria monocytogenes contamination. Affected packages have lot codes beginning with 'N' or 'Y' with 'Best if Used By' dates from November 30, 2021 to January 8, 2022.

    Product
    Ahold 12oz Garden Salad Mix Product UPC 688267184437
    Category
    Food
    Distribution
    36 states