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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26476–26500 of 90150

  • SevereNHTSA·22E018000·2022-03-11

    Norco Frames Recalled for Improperly Welded Couplers

    Norco Industries is recalling certain frames with Model CA-5400 couplers due to improper welding that may cause trailer separation.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V150000·2022-03-11

    Ford Recalls F-150, Expedition, Navigator for Brake Master Cylinder Leak

    Ford is recalling 2016-2018 F-150, 2016-2017 Expedition, and Navigator vehicles because a brake master cylinder leak may reduce front brake function and increase crash risk.

    Product
    FORD — FORD, LINCOLN F-150, EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V143000·2022-03-11

    Forest River 2022 Travel Trailers Recalled for Coupler Weld Defect

    Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.

    Product
    FOREST RIVER — FOREST RIVER, EAST TO WEST XLR TOYHAULER, SILVER LAKE, VIBE, DELLA TERRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V145000·2022-03-11

    2020-2022 Ford F-59 Steering Shaft Bolt May Loosen, Increasing Crash Risk

    The bolt securing the intermediate steering shaft to the steering gear box may become loose, potentially causing loss of steering control and increased crash risk. Ford is replacing the bolts for free.

    Product
    FORD — FORD F-59
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V149000·2022-03-11

    2022 Ford Escape High Voltage Battery Failure Causes Drive Power Loss

    The high voltage battery in 2021-2022 Ford Escape and 2022 Lincoln Corsair hybrid vehicles may fail, causing sudden loss of drive power and increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD CORSAIR, ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V144000·2022-03-11

    Keystone Travel Trailers Recalled for Faulty Wiring Disabling Safety Alarms

    Keystone is recalling 2021-2022 Sprinter and Bullet models plus multiple 2022 travel trailer and fifth-wheel variants due to faulty solar controller wiring that can disable carbon monoxide and propane gas detectors.

    Product
    KEYSTONE — KEYSTONE MONTANA HIGH COUNTRY, COUGAR, CARBON, BULLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V151000·2022-03-11

    2021-2022 Ford Edge Rearview Camera Software Error Causes Display Failure

    Ford is recalling 2021-2022 Edge vehicles with a software error that may cause the rearview camera to display a blank or distorted image. This reduces driver visibility behind the vehicle, increasing crash risk.

    Product
    FORD — FORD EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03102022-01·2022-03-10

    Trader Joe's Chicken Salad Recalled for Potential Hard Plastic Contamination

    USDA FSIS issued a public health alert for Trader Joe's Crunchy Slaw with Chicken due to potential hard plastic in the dressing. No illnesses have been reported.

    Product
    R & G Fine Foods, Inc. — FSIS Issues Public Health Alert for Chicken Salad Products Containing FDA-Regulated Dressing that has been Recalled due to Foreign Material Contamination
    Category
    Food
    Distribution
    5 states
  • HighNHTSA·22V141000·2022-03-10

    GMC Recalls 2022 Hummer EV Pickup for Taillight Software Defect

    General Motors is recalling 2022 GMC Hummer EV Pickups because taillight software may cause lights to fail or stay on, increasing crash risk.

    Product
    GMC — GMC HUMMER EV PICKUP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E017000·2022-03-10

    Chrysler Recalls Mopar ABS Modules for Electronic Stability Control Defect

    Chrysler is recalling Mopar Anti-lock Brake System (ABS) Control Modules because software may prevent the Electronic Stability Control (ESC) malfunction light from illuminating, increasing crash risk.

    Product
    ELECTRONIC STABILITY CONTROL (ESC) recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0815-2022·2022-03-09

    Vadilal Quick Treat Custard Apple Pulp Recalled for Salmonella

    Vadilal Industries is recalling Quick Treat Custard Apple Pulp (1kg packages, UPC 8901777282168) due to potential Salmonella contamination. Approximately 997 cases were distributed nationwide to retail stores.

    Product
    Vadilal Quick Treat Custard Apple Pulp Net Wt, 1kg/35.27-oz. Product code FPEP44302 UPC:8901777282168 Best Before September 2023
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0806-2022·2022-03-09

    Whole Foods Market Vanilla Shortbread Cookies Recalled Due to Undeclared Egg

    Whole Foods Market Vanilla Shortbread Cookies are recalled due to undeclared egg allergen. The 23 units distributed in Washington D.C. with pack date 1/20/22 may pose serious risk to consumers with egg allergies.

    Product
    Whole Foods Market Vanilla Short Bread Cookies packaged in clear plastic container with a white scale label applied PLU 66705
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0680-2022·2022-03-09

    Celltrion DiaTrust COVID-19 Rapid Test Kits Recalled for Unauthorized Clinical Use

    Celltrion USA recalled COVID-19 rapid test kits (DiaTrust) in a Class I action. The kits are labeled for research use only, but the firm assured distributors they could be used for clinical diagnosis, which is not authorized.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0663-2022·2022-03-09

    Philips Respironics V60 Plus Ventilators with Defective Adhesive Recalled

    Respironics California is recalling 294 V60 Plus ventilators assembled with expired adhesive. The adhesive may fail, causing the bracket to loosen and damage capacitors, potentially stopping ventilation delivery.

    Product
    Philips Respironics V60 Plus Ventilator Part Number 1138747
    Category
    Medical Device
    Distribution
    13 states
  • SevereNHTSA·22V139000·2022-03-09

    Maintainer Recalls 2021-2022 Crane Trucks Due to Fire Risk

    Maintainer is recalling 2021-2022 crane-equipped truck bodies because an inductor may contact the frame, causing an electric arc and increasing fire risk.

    Product
    MAINTAINER — MAINTAINER CRANE W/ SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0659-2022·2022-03-09

    COVID-19 Rapid Test Kits Recalled for Risk of False Positive Results

    Celltrion DiaTrust COVID-19 Ag Rapid Test kits from lot COVGCCM0008 are being recalled due to reports of false positive results. The affected 243 kits were distributed to six states before the recall.

    Product
    Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
    Category
    Medical Device
    Distribution
    6 states
  • SevereFDA (Devices)·Z-0662-2022·2022-03-09

    Philips V60 Ventilator Recall: Expired Adhesive May Cause Device Failure

    A limited number of Philips Respironics V60 ventilators were assembled with expired adhesive. If the adhesive fails, the ventilator could stop providing ventilation.

    Product
    Philips Respironics V60 Ventilator Part Number 1053617
    Category
    Medical Device
    Distribution
    13 states
  • SevereFDA (Food)·F-0813-2022·2022-03-09

    Enoki Mushrooms Recalled Due to Listeria monocytogenes Contamination Risk

    GOLDEN MEDAL MUSHROOM INC is recalling Xuerong brand enoki mushrooms contaminated with Listeria monocytogenes. The affected product was distributed in California, Texas, and Illinois.

    Product
    Enoki Mushrooms, brand Xuerong, net wt. 150 g/ 5.25200g/7.05-ounce packages, UPC 6953150110157. 34 0er carton.
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·22094·2022-03-09

    Olight M2R Pro and Warrior Mini Flashlights Recalled for Burn Hazard

    Olight is recalling about 215,100 M2R Pro and Warrior Mini flashlights because they can turn on accidentally and overheat while stored in a holster or pocket, creating a burn hazard. The company has received 127 reports of unintended activation with 22 burn injuries, including three second-degree burns.

    Product
    M2R Pro and Warrior Mini Flashlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0720-2022·2022-03-09

    BUTLER Clear Dip Recalled for Lack of FDA Premarket Clearance

    Sunstar Americas is recalling BUTLER Clear Dip nationwide due to lack of FDA premarket clearance. The product was distributed in 22,514 units across multiple lot codes.

    Product
    BUTLER Clear Dip, 12 bottles/case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0689-2022·2022-03-09

    Titanium Toe Joint Implant Labeling Error: Unvalidated MRI Safety Claims

    BioPro Titanium MPJ toe implants are recalled due to false documentation claiming MRI safety testing that was never performed. Patients should not undergo MRI with this implant until properly evaluated.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM PC LG, Part ID 17038
    Category
    Medical Device
    Distribution
    Distributed nationwide