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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6926–6950 of 36563

  • SevereNHTSA·22V926000·2022-12-14

    Polestar Recalls 2020-2021 Polestar 1 Vehicles for Battery Fire Risk

    Polestar is recalling 2020-2021 Polestar 1 vehicles because defective high-voltage battery cells may overheat and cause a fire. Dealers will replace the cells.

    Product
    POLESTAR — POLESTAR POLESTAR 1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0338-2023·2022-12-14

    FDA Class I Recall: CAIRE Liberator 30 Liquid Oxygen System Units

    Caire, Inc. is recalling five CAIRE Liberator 30 liquid oxygen system units due to weld defects on the inner bottle that could lead to device failure and loss of oxygen supply to dependent patients.

    Product
    CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0327-2023·2022-12-14

    Thermo Sensititre diagnostic plate recalled for false susceptibility results

    Sensititre diagnostic plates may give false antibiotic susceptibility results for certain bacteria species, potentially affecting treatment decisions. The FDA issued a Class I recall for approximately 1,917 units distributed nationwide.

    Product
    Thermo SCIENTIFIC Sensititre Plate, GN4F, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E099000·2022-12-14

    Williamsen-Godwin Recalls Trailers with Fracturing Steering Arms

    Williamsen-Godwin is recalling specific trailers equipped with Smart-Steer 2.0 axles because the steering arm may fracture. This defect can cause parts to separate, increasing the risk of a crash.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0323-2023·2022-12-14

    Dewei DNA/RNA Preservation Kits recalled for lack of FDA authorization

    Dewei DNA/RNA Preservation Kits (catalog DW-80005-1B) were distributed in the U.S. without FDA authorization or clearance. Approximately 1,348,000 units were distributed to California, Florida, Kentucky, and Michigan.

    Product
    Dewei DNA/RNA Preservation Kit, Catalog number DW-80005-1B
    Category
    Medical Device
    Distribution
    4 states
  • SevereFDA (Devices)·Z-0328-2023·2022-12-14

    Medical Device Recall: Sensititre GN6F May Report False Antibiotic Susceptibility Results

    The FDA recalled Sensititre GN6F Gram Negative antimicrobial susceptibility test plates (2,471 units) because they may report false results indicating bacteria are susceptible to certain antibiotics when they are actually resistant.

    Product
    Thermo SCIENTIFIC, Sensititre GN6F, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0329-2023·2022-12-14

    Sensititre GN7F Antibiotic Test Plates Recalled for Inaccurate Susceptibility Results

    Remel Inc. recalled 8,073 units of Sensititre GN7F antibiotic susceptibility test plates after discovering they may report false results for certain bacteria, potentially leading to incorrect antibiotic treatment decisions.

    Product
    Thermo SCIENTIFIC, Sensititre GN7F, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0332-2023·2022-12-14

    FDA Class I Recall: Thermo Sensititre Gram Negative Diagnostic Test Inaccuracy

    Thermo Scientific Sensititre CMC7AFLF Gram Negative diagnostic tests may produce false susceptible results for certain bacteria, potentially leading to ineffective antibiotic treatment decisions. The FDA has classified this as a Class I recall.

    Product
    Thermo SCIENTIFIC, Sensititre CMC7AFLF, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0337-2023·2022-12-14

    Liquid Oxygen System Devices Recalled Due to Weld Quality Issues

    Caire Inc. is recalling 70 CAIRE Liberator 45 liquid oxygen systems due to inconsistencies in weld penetration on the inner bottle's longitudinal weld seam discovered during an audit.

    Product
    CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0335-2023·2022-12-14

    Medical Device Recall: Sensititre Test Produces False Antibiotic Susceptibility Results

    Remel Inc. is recalling a diagnostic test that may incorrectly report antibiotic susceptibility in certain Gram-negative bacteria. False results could lead to inappropriate antibiotic treatment.

    Product
    Thermo SCIENTIFIC, Sensititre STP7F, Gram Negative IVD AST
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0183-2023·2022-12-14

    Enoki Mushroom Recall Due to Listeria monocytogenes Contamination

    GREEN DAY PRODUCE is recalling enoki mushrooms (UPC 16430-69080) due to Listeria monocytogenes contamination. Affected products were distributed to retailers and distributors in 12 states.

    Product
    Enoki Mushroom Net wt. 200g (7.05 oz.) 25 units per case UPC: 16430-69080 Keep refrigerated Product of Korea
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·22V928000·2022-12-14

    2022 Ford Bronco Airbag Sensors May Not Secure Properly

    Ford is recalling certain 2022 and 2021 Bronco vehicles because the side impact sensors may not be properly secured. This could cause airbags to deploy unintentionally or fail to deploy in a crash, increasing injury risk.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V927000·2022-12-14

    Audi Recalls 2022 E-Tron GT Models Due to Suspension Strut Defect

    Audi is recalling 96 2022 E-Tron GT vehicles because a retaining ring on the front suspension strut may come loose, potentially causing air loss and loss of vehicle control.

    Product
    AUDI — AUDI E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V921000·2022-12-13

    2021 Porsche Taycan Suspension Strut Defect May Cause Loss of Vehicle Control

    A retaining ring on the 2021 Porsche Taycan's suspension strut may come loose, causing loss of vehicle control and increasing crash risk. Repairs will be provided free by Porsche dealers.

    Product
    PORSCHE — PORSCHE TAYCAN, TAYCAN 4S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V917000·2022-12-12

    Volvo Bus 9700 Recalled for GPS Installation Defect

    Volvo Bus is recalling 2022 9700 buses because incorrectly installed GPS devices may cause accelerator sensor malfunction and loss of drive power.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V905000·2022-12-08

    Hyundai Translead Recalls 2020-2021 Trailers Due to Brake Pad Retaining Clip Defect

    Hyundai Translead is recalling 2020-2021 Dry Van and Reefer Trailers because a loose brake pad retaining clip may detach, reducing brake performance or causing a flat tire.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD REEFER TRAILER, DRY VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V908000·2022-12-08

    2023 McLaren Artura recalled for fuel pipe defect increasing fire risk

    McLaren is recalling 164 2023 Artura vehicles because high-pressure fuel pipe nuts may loosen, causing fuel leaks that could lead to fires. Dealers will replace the fuel pipes at no cost.

    Product
    MCLAREN — MCLAREN ARTURA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V906000·2022-12-08

    2023 KIA Forte front left steering knuckle may crack

    Kia is recalling certain 2023 Forte vehicles due to a manufacturing error that may cause the front left steering knuckle to crack, resulting in loss of steering control and increased crash risk.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V910000·2022-12-08

    Navistar Recalls 2023 IC CE and IN RE Buses for Axle Fastener Issue

    Navistar is recalling 2023 IC CE and IN RE commercial buses because incorrectly tightened fasteners may allow the rear axle to shift, increasing crash risk.

    Product
    IC BUS — IC BUS, INTERNATIONAL CE, RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23065·2022-12-08

    Ortal Gas Fireplaces Recalled Due to Fire Hazard Risk

    Ortal USA is recalling about 400 Traditional 90 and Traditional 110 gas fireplaces due to improper installation that can cause fire hazards. The firm has received four reports of installation errors resulting in fires with property damage.

    Product
    Traditional 90 and Traditional 110 Gas Fireplaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23064·2022-12-08

    3M Scotch TL1302 Thermal Laminators Recalled Due to Fire Hazard

    3M is recalling approximately 516,500 Scotch TL1302 Thermal Laminators because a safety feature can malfunction when the device overheats, posing a fire hazard. The company has received nine reports of the laminators catching fire, with three reports of minor property damage but no injuries.

    Product
    Scotch TL1302 Thermal Laminators
    Category
    Consumer Product
    Distribution
    Distributed nationwide