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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25601–25625 of 90145

  • HighFDA (Food)·F-1049-2022·2022-05-18

    Jerk Dressing Recalled for Salmonella Contamination in Yellow Onion

    Mosaic Food Company is recalling refrigerated Jerk Dressing made with yellow onions that were recalled for Salmonella contamination. The product was distributed in California.

    Product
    Jerk Dressing; Made with Yellow Onion Item number 7028, 7029 Refrigerated
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1049-2022·2022-05-18

    Bronchovideoscope Recall for Updated Sterilization and Reprocessing Instructions

    Olympus bronchovideoscopes are recalled due to updates required for proper sterilization and reprocessing procedures. Healthcare providers must follow new instructions for chemical disinfection and ETO gas sterilization.

    Product
    BF-1TQ180: EVIS EXERA II Bronchovideoscope
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0854-2022·2022-05-18

    Xanax XR Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Viatris Inc recalls Xanax XR (alprazolam) 3 mg extended-release tablets due to failed dissolution specifications. Affected tablets may not break down properly, potentially reducing medication effectiveness.

    Product
    Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer Inc, NY, NY 10017, NDC 0009-0068-07.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1062-2022·2022-05-18

    CMOS Video Cysto-Urethroscope Disinfection Failure Puts Patients at Infection Risk

    Karl Storz Endoscopy is recalling CMOS Video Cysto-Urethroscope devices because they fail to achieve adequate microbial reduction during disinfection, creating infection risk.

    Product
    11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS VIDEO-CYSTO-URETHROSCOPE REV; 11272VU 11272VUK CMOS VIDEO-CYSTO-URETHROSCOPE US; 11272VUA 11272VUAK CMOS VIDEO-CYSTO-URETHROSCOPE US
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1068-2022·2022-05-18

    Karl Storz Video Ureteroscopes May Not Be Properly Sterilized

    Karl Storz ureteroscopes and flexible video ureteroscopes may fail to achieve adequate sterilization during the disinfection process, potentially leaving microorganisms on the devices that could cause patient infections.

    Product
    11278V 11278VK CMOS Video Ureteroscope Z17744US-A (04/2016); 11278VA 11278VAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA (10/2020); 11278VU 11278VUK Flexible Video-Uretero-Renoscope (FLEX-XC) Z18447US-BC (03/2018); 11278VUA 11278VUAK Flexible…
    Category
    Medical Device
    Distribution
    52 states
  • HighFDA (Devices)·Z-1052-2022·2022-05-18

    Prothrombin Time Reagent Recalled for Quality Control Failures

    Instrumentation Laboratory is recalling HemosIL ReadiPlasTin due to variable and out-of-specification quality control results. The manufacturer is removing all affected lots and providing customers with an alternative reagent.

    Product
    HemosIL ReadiPlasTin, Part No. 0020301400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-05182022-01·2022-05-18

    USDA Issues Public Health Alert for Underprocessed Ready-to-Eat Ham

    USDA FSIS issued a public health alert for Great Value Black Forest Ham that may not be fully cooked. Consumers should discard the product.

    Product
    JBS Prepared Foods — FSIS Issues Public Health Alert for Ready-To-Eat Ham Product Due to Possible Processing Deviation
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1042-2022·2022-05-18

    Medtronic IN.PACT Admiral balloon catheters recalled for damaged packaging

    Medtronic is recalling IN.PACT Admiral paclitaxel-coated balloon catheters due to damaged packaging that may result in loss of sterility, affecting approximately 6,035 units worldwide.

    Product
    Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model Numbers:ADM04004013P ADM04008013P ADM04008013P ADM04008013P ADM04012013P ADM04015013P ADM04015013P ADM04025013P ADM05004013P ADM05004013P ADM05006013P ADM05006013P…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1058-2022·2022-05-18

    ProterixBio SARS-CoV-2 Antibody Test Recalled for Inaccurate Results

    ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test kits are being recalled due to insufficient clinical performance data. The FDA determined test results may not be accurate, with potential false positives or false negatives.

    Product
    ProterixBio SARS-CoV-2 (RBD) IgG Antibody Test, and associated ProterixBio Dried Blood Spot Collection Kit, no model number
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Devices)·Z-1037-2022·2022-05-18

    Surgical Device Kits Recalled Due to Improper Sterilization Process

    American Contract Systems is recalling ACS Arthroscopy, Knee, and Hand surgical kits because they were sterilized using a higher than specification ethylene oxide concentration.

    Product
    1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0859-2022·2022-05-18

    Hand Sanitizer Product Recalled Due to Acetaldehyde Contamination

    Kill 'Dat Sanitizing Products Hand Sanitizer (1 gallon, Batch 39) recalled because acetaldehyde levels exceed manufacturer specifications. Product distributed in Louisiana.

    Product
    Kill 'Dat Sanitizing Products Hand Sanitizer, 1 gallon (128 fl. oz.) 80% Alcohol, OTC, Manufactured by: Lula Holdings LLC, 15532 St. Charles Avenue, New Orleans, LA, NDC 77348-001-02.
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·22V346000·2022-05-17

    2021 Ford Expedition and Navigator: Engine Compartment Fire Risk Recall

    Ford is recalling certain 2021 Expedition and Lincoln Navigator vehicles due to risk of engine compartment fire while driving or parked. Owners should park vehicles outside away from structures until repairs are available.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V343000·2022-05-17

    2020-2023 Trailstar and Ranger Trail Boat Trailers Recalled for Hub Seizure

    Tracker Marine is recalling 2020-2023 Trailstar and Ranger Trail boat trailers because axle hubs were not tightened properly, which can cause hub seizure and loss of vehicle control.

    Product
    TRAILSTAR — TRAILSTAR, RANGER TRAIL BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V344000·2022-05-17

    2022 Kia Telluride recall: instrument cluster display may go blank

    Excess adhesive in the instrument cluster circuit board may cause the display to go blank, preventing drivers from seeing critical information and increasing crash risk.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V340000·2022-05-16

    FCCC MT50E Vans Recalled for Shift Knob Malfunction

    Daimler Trucks North America is recalling 2021-2022 FCCC MT50E walk-in vans because a faulty shift knob may cause unintended movement.

    Product
    FCCC — FCCC MT50E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E039000·2022-05-16

    Carparts.com Recalls Oil Filter Housings Due to Leak and Fire Risk

    Carparts.com is recalling specific oil filter housings because a seal defect may cause oil leaks, increasing the risk of fire or engine failure.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION:FILTER/SCREEN recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V339000·2022-05-16

    2022 Freightliner Cascadia trucks recalled for disabled antilock brakes and stability control

    Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V338000·2022-05-16

    Commercial trucks recalled for incorrect gross axle weight labels

    Daimler Trucks is recalling commercial trucks with incorrect weight-rating labels that could allow unsafe overloading. Dealers will replace the labels free of charge.

    Product
    WESTERN STAR — WESTERN STAR, FREIGHTLINER 4900, 4700, 5700, NEW CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V342000·2022-05-16

    Bowlus Endless Highways Travel Trailers Recalled for Gas Leak Risk

    Bowlus is recalling 2022 Endless Highways travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.

    Product
    BOWLUS — BOWLUS ENDLESS HIGHWAYS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V341000·2022-05-16

    Utilimaster Walk-in Van Recall for Incorrect Tire Placard Information

    Shyft Group is recalling 2022 Utilimaster Walk-in vans because tire size and pressure labels may be incorrect, potentially leading to improper tire inflation.

    Product
    UTILIMASTER — UTILIMASTER WALK-IN VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V333000·2022-05-13

    Ford Recalls 2021 Mustang Mach-E Vehicles for Software Defect

    Ford is recalling 2021 Mustang Mach-E all-wheel drive vehicles because a software error may cause unintended acceleration or loss of power.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V337000·2022-05-13

    Ford Recalls 2016 Super Duty Trucks for Air Bag Defect

    Ford is recalling 2016 Super Duty trucks because dust in the steering wheel clock spring may prevent the driver's air bag from deploying.

    Product
    FORD — FORD F-350 SD, F-550 SD, F-450 SD, F-250 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide