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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16501–16525 of 89775

  • HighFDA (Devices)·Z-0060-2024·2023-11-01

    Diagnostic Test Strips Recalled for Manufacturing Conformance and Documentation Issues

    Universal Meditech Inc. is recalling diagnostic test strips due to Quality System violations and lack of manufacturing documentation. The company is closing and cannot provide post-market surveillance or support.

    Product
    DiagnosUS¿ One Step FSH Menopausal Test (Strip) REF 210-07
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0138-2024·2023-11-01

    Radiological Imaging Software May Display Images from Multiple Patients in Single Study

    GE Healthcare is recalling Centricity PACS-IW radiological imaging software versions V3.7.x through 3.7.3.9 SP3 because images from different patients may appear together in a single study, risking patient misidentification.

    Product
    Centricity PACS-IW, software versions V3.7.x through 3.7.3.9 SP3; Radiological Image Processing System
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0301-2024·2023-11-01

    Dark Chocolate Peanut Butter Recalled for Undeclared Sesame Allergen

    Betty Lou's Inc. recalls Stabilyze Sugar Stable Dark Chocolate Peanut Butter due to undeclared sesame. The product was distributed across 26 states; consumers with sesame allergies should not consume it.

    Product
    Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UPC 0 16073 00213 1. There are 12 packages per display box (box UPC 0 16073 00223 0). The label allergens contains statement declares Milk, Peanut, Tree Nuts…
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0155-2024·2023-11-01

    SOZO Bilateral Arm L-Dex Software inadequate lymphedema detection sensitivity

    Impedimed's SOZO Bilateral Arm L-Dex Software (versions 4.1 and 5.0) has inadequate sensitivity for detecting early lymphedema, which could delay treatment. The FDA is recalling 354 units distributed nationwide.

    Product
    SOZO Bilateral Arm L-Dex Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0049-2024·2023-11-01

    Pregnancy Test Recalled for Unverified Manufacturing Compliance and Firm Closure

    Universal Meditech Inc. is recalling the Am I Pregnant? One Step HCG Pregnancy Test because the company is going out of business and cannot verify manufacturing compliance or provide quality system documentation.

    Product
    Am I Pregnant? One Step HCG Pregnancy Test REF 100-17
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0180-2024·2023-11-01

    Sub Q Recorder Pack components may lose functionality due to improper sterilization

    American Contract Systems is recalling Sub Q Recorder Pack components that were improperly sterilized using ethylene oxide at excessive temperatures. The I.V. Cath and Dermabond components may lose functionality or drug efficacy as a result.

    Product
    Sub Q Recorder Pack, REF BPRC87A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23E085000·2023-11-01

    Hollywood Racks Recalls 2022-2023 Destination E Rack Bicycle Carriers

    Hollywood Racks is recalling 2022-2023 Destination E Rack Bicycle Carriers because a component may fail, allowing a bike to detach and become a road hazard.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2024·2023-11-01

    Pregnancy test strips recalled due to manufacturing documentation gaps

    Universal Meditech Inc. is recalling To Life hCG pregnancy test strips because the company is ceasing operations and cannot verify manufacturing compliance. The firm cannot provide documentation of manufacturing standards, storage conditions, or post-market safety monitoring.

    Product
    To Life hCG Pregnancy Urine Test Strips Format REF Cat No: 100-10
    Category
    Medical Device
    Distribution
    8 states
  • SevereUSDA FSIS·055-2023·2023-10-31

    Q'Delicia Recalls Ready-to-Eat Empanada Products Produced Without Inspection

    Q'Delicia is recalling ready-to-eat empanada products produced without federal inspection. The products were distributed in Florida and may not be safe for consumption.

    Product
    Q'Delicia Recalls Ready-To-Eat Empanada Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·23V730000·2023-10-31

    Triumph Rocket 3 rear brake master cylinders may extend stopping distance

    Triumph is recalling certain 2020-2024 Rocket 3 motorcycles because the rear brake master cylinder may fail to move fluid properly, requiring an extended distance to stop. 3,557 units affected.

    Product
    TRIUMPH — TRIUMPH ROCKET 3 R, ROCKET 3 GT, ROCKET 3 TFC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23T007000·2023-10-31

    Toyo Recalls Open Country and Extensa Tires Due to Mold Defect

    Toyo Tire Holdings is recalling certain Open Country and Extensa tires because they may have been produced with the wrong mold, risking tread or sidewall detachment.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V726000·2023-10-30

    Starcraft and Glaval Transit Buses Recalled for Air Compressor Defect

    Forest River Bus is recalling certain 2021-2023 Starcraft and Glaval transit buses because the air conditioning compressor may contact the sway bar, risking loss of steering control.

    Product
    STARCRAFT BUS — STARCRAFT BUS, GLAVAL BUS ALLSTAR XL, ALLSTAR XLT, CONCORDE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·054-2023·2023-10-30

    Olymel Recalls Ready-to-Eat Ham Products Imported Without Reinspection

    Olymel is recalling approximately 11,016 pounds of ready-to-eat ham products that were imported into the United States without the required import reinspection.

    Product
    Olymel Recalls Ready-To-Eat Ham Products Imported Without the Benefit of Import Reinspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·23V727000·2023-10-27

    Ford Mustang Brake Fluid Warning System Software Recall

    Ford is recalling 2020-2023 Mustang vehicles because the brake fluid level sensor may fail to illuminate the warning light when brake fluid is low. Drivers could operate the vehicle with insufficient brake fluid, reducing braking performance and increasing crash risk.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V722000·2023-10-26

    New Flyer Transit Buses Recalled for Transmission Yoke Separation Risk

    New Flyer is recalling 2019-2024 transit buses because the transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XN40, XN35, XD35, XD40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E084000·2023-10-26

    Akron Brass Recalls Vehicle Multiplex Systems Due to Fire Risk

    Weldon Division of Akron Brass is recalling 8x16 Input-Output Node Vehicle Multiplex Systems because a wiring failure could cause overloaded circuits and fire.

    Product
    ELECTRICAL SYSTEM:WIRING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24013·2023-10-26

    Best Buy Recalls Insignia Pressure Cookers Due to Burn Hazard

    Best Buy is recalling about 930,000 Insignia pressure cookers because incorrect volume markings on the inner pot can cause consumers to overfill the unit, leading to hot food and liquids being ejected and causing burn injuries.

    Product
    Insignia pressure cookers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V719000·2023-10-26

    Mazda Recalls 2024 CX-90 Plug-in Hybrids for Software Error

    Mazda is recalling 2024 CX-90 plug-in hybrid vehicles because a software error may cause the engine and electric motor to shut down unexpectedly, resulting in a loss of drive power.

    Product
    MAZDA — MAZDA CX-90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V723000·2023-10-26

    2024 Subaru Forester Water Pipe Bolts May Loosen, Risk Fire

    Certain 2024 Subaru Forester models have engine water pipe attachment bolts that may loosen, allowing the pipe to leak coolant onto hot engine components and create a fire risk.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V716000·2023-10-26

    Third-row seatbelt buckle defect in 2022–2024 Jeep Wagoneer models

    Chrysler is recalling 2022–2024 Jeep Wagoneer and Grand Wagoneer vehicles because the third-row seatbelt buckles may not fasten properly. Unfastened seatbelts could increase injury risk during a crash.

    Product
    JEEP — JEEP WAGONEER, GRAND WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide