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 the agency’s own highest classification or reported deaths or serious injuries, 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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26651–26675 of 90158

  • HighFDA (Devices)·Z-0675-2022·2022-03-02

    Biomet Shoulder Implant Stem Coating Adhesion Defect Recall

    Biomet is recalling shoulder implant stems due to improper rework of porous plasma coating, which may lack sufficient adhesion strength. Affected units may fail if the coating detaches.

    Product
    Comprehensive Shoulder System Mini Humeral Stem, Porous Plasma, 12 MM, 83 MM Long Item Number: 113632
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0741-2022·2022-03-02

    Arillis Tortillas Recalled Due to Undeclared Wheat Allergen

    Arillis Corp is recalling Tortillas Arillis due to undeclared wheat. Consumers with wheat allergies may be at risk if they consume the product.

    Product
    Tortillas Arillis, Arillis Corp, Contains: 10 (ten) tortillas
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0801-2022·2022-03-02

    Diastatic Malt Powder Recalled Due to Potential Salmonella Contamination

    Malt Products Corporation is recalling approximately 3,015 bags of Diastatic Malt Powder due to potential Salmonella contamination. The affected product was distributed to multiple states; consumers should not consume it.

    Product
    Diastatic Malt Powder 50lb bag - up to 50 bags per pallet Malt Products Corporation
    Category
    Food
    Distribution
    14 states
  • SevereNHTSA·22E015000·2022-03-01

    Marion Body Works Recalls Emergency Vehicles Due to Fuel Leak Risk

    Marion Body Works is recalling specific 2018-2021 emergency vehicles because a fuel rail defect may cause leaks, increasing fire risk.

    Product
    MARION BODY WORKS — MARION BODY WORKS FREIGHTLINER M2, KENWORTH T3 SERIES, INTERNATIONAL SR525
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03012022-01·2022-03-01

    Ready-to-Eat Meat Products Recalled for Undeclared Wheat Allergen

    USDA FSIS issued a public health alert for ready-to-eat meat products containing a seasoning mix with undeclared wheat. Consumers are advised not to consume these items.

    Product
    FSIS Issues Public Health Alert for Ready-to-Eat Meat Products Containing FDA-Regulated Seasoning Mix That Has Been Recalled Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V116000·2022-03-01

    Pierce Arrow XT Firetruck Recall for Improperly Crimped Lifting Cables

    Pierce Manufacturing is recalling one 2021 Arrow XT firetruck because improperly crimped lifting cables could cause the generator set to fall, increasing injury risk.

    Product
    PIERCE — PIERCE ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V114000·2022-02-28

    Proterra buses recalled for loose steering gearbox securing bolts

    Proterra is recalling 2017-2022 Catalyst and ZX5 buses because steering gearbox securing bolts may loosen due to insufficient adhesive, risking loss of steering control. Owner notifications were sent October 7, 2022.

    Product
    PROTERRA — PROTERRA ZX5, CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V112000·2022-02-25

    Mercedes-Benz Recalls 2022 EQS Models Due to Electrical Fire Risk

    Mercedes-Benz is recalling 2022 EQS 450, EQS 580, and AMG EQS 53 vehicles because improperly secured electrical connections may increase the risk of a fire or cause headlight failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, AMG EQS 53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V109000·2022-02-24

    Ford Recalls 2021 Escape Hybrid Vehicles Due to Crankshaft Defect

    Ford is recalling 2021 Escape Hybrid vehicles because an incorrectly manufactured engine crankshaft may cause engine damage, leading to stalling or fire.

    Product
    FORD — FORD ESCAPE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V108000·2022-02-24

    Tenco Recalls One TOR DR-106100 Highway Carrier for Fuel Leak Risk

    Tenco Inc. is recalling one 2020 TOR DR-106100 highway carrier because fuel tubes may crack, causing a high-pressure fuel leak that increases fire risk.

    Product
    TOR — TOR DR-106100
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V107000·2022-02-24

    2021 Toyota C-HR: Inoperative Radar Sensor Disables Collision Avoidance

    Certain 2021 Toyota C-HR vehicles have a radar sensor that was not activated during production, disabling the pre-collision system and forward collision avoidance. Dealers will activate the sensor at no cost.

    Product
    TOYOTA — TOYOTA C-HR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22731·2022-02-24

    Kelly Wynne Children's Handbags Recalled for Excess Lead Content

    Kelly Wynne is recalling about 1,050 Mama & Me MINI children's handbags sold online from July 2020 through October 2021 because metal components contain lead levels that exceed the federal ban. No injuries have been reported.

    Product
    Mama & Me MINI Children's Handbags
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V110000·2022-02-24

    Yamaha Recalls 2021 Tracer 9 GT Motorcycles Due to Throttle Grip Defect

    Yamaha is recalling 453 2021 Tracer 9 GT motorcycles because the throttle grip may break if used to lift the bike, potentially causing loss of throttle control and a crash.

    Product
    YAMAHA — YAMAHA TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V111000·2022-02-24

    Missing Mounting Bolt in 2022 INFINITI QX60 Second-Row Seat Track

    Nissan is recalling 2022 INFINITI QX60 vehicles because the second-row seat track may be missing a mounting bolt. This could allow the seat track to move during a crash, increasing injury risk.

    Product
    NISSAN — NISSAN, INFINITI PATHFINDER, QX60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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 (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-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
  • SevereNHTSA·22V104000·2022-02-23

    Tesla Model S Side Curtain Air Bag Inflator Defect

    Tesla is recalling 2021-2022 Model S vehicles due to side curtain air bag inflators that may have been assembled incorrectly. This could cause delayed air bag deployment during a crash, increasing injury risk.

    Product
    TESLA — TESLA MODEL S
    Category
    Vehicle
    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 (Devices)·Z-0627-2022·2022-02-23

    Arrow-Trerotola Percutaneous Thrombolytic Device catheter tips may separate during use

    The FDA is recalling Arrow-Trerotola Percutaneous Thrombolytic Device catheters due to reports of tip separation during use. Approximately 3,668 units were distributed worldwide.

    Product
    Arrow-Trerotola PTD Set (Percutaneous Thrombolytic Device), PT-45509 containing components: PT-45509-S6, PT-45509-T The Arrow-Trerotola Percutaneous Thrombolytic Device (PTD) Catheter, in conjunction with the Arrow Rotator Drive Unit, permits mechanical declotting of native…
    Category
    Medical Device
    Distribution
    Distributed nationwide