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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801–825 of 90235

  • HighFDA (Devices)·Z-3032-2026·2026-09-02

    Healthmark Protein Test Recalled Due to Expired Ingredient

    Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.

    Product
    healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3029-2026·2026-09-02

    Medline Recalls Neurosurgical Convenience Kits Due to Contamination

    Medline Industries is recalling 241 neurosurgical convenience kits distributed nationwide because they contain a potentially contaminated component.

    Product
    Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0777-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 75 mcg tablets nationwide because they may contain less than the labeled amount of active ingredient.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0781-2026·2026-09-02

    Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide

    Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 125 mcg tablets because they are subpotent. The recall is ongoing nationwide.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3012-2026·2026-09-02

    Midmark IQecg Digital ECG Software Recall for Inaccurate Waveforms

    Midmark is recalling IQecg Digital ECG software due to a communication anomaly that may cause incorrect waveforms and inaccurate heart rate calculations.

    Product
    Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3026-2026·2026-09-02

    Medline C-Section Convenience Kits Recalled for Contaminated Components

    Medline Industries is recalling 106 C-section convenience kits distributed nationwide due to potentially contaminated components.

    Product
    Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755; 3) AHR C-SECTION KIT, Medline Kit SKU DYNJ912014.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3005-2026·2026-09-02

    Halyard DAVINCI TRUCUSTOM Foley Catheter Kits Recalled for Latex Labeling Deficiency

    AVID Medical is recalling 45 Halyard DAVINCI TRUCUSTOM Foley catheter kits because the labeling fails to identify that the statlock component contains natural rubber latex.

    Product
    Brand Name: Halyard Product Name: DAVINCI TRUCUSTOM BUNDLE containing TRAY FOLEY 16FR W/STATLOCK Model/Catalog Number: SAMM064-27
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3023-2026·2026-09-02

    Medline Convenience Kits Recalled for Potentially Contaminated Component

    Medline Industries is recalling 15 convenience kits (SKU CDS980375M) due to a potentially contaminated component. The kits were distributed in 18 US states.

    Product
    Medline convenience kits labeled as: LTP CDS-LF, Medline kit SKU CDS980375M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3039-2026·2026-09-02

    GE Medical Systems Recalls Portrait Core Services Software Reload Unit

    GE Medical Systems is recalling a software reload unit for the Portrait Core Services system due to a defect that may cause loss of patient monitoring and reset alarm settings.

    Product
    FRU (Field replaceable unit), PORTRAIT CORE SERVICES SW RELOAD V1.1, Ref# 5700225
    Category
    Medical Device
    Distribution
    2 states
  • SevereNHTSA·26V567000·2026-09-01

    Peterbilt Recalls 2027 548 Trucks Due to Brake Valve Size Issues

    PACCAR is recalling 2027 Peterbilt 548 trucks because incorrect front brake valve and hose sizes may delay brake response, increasing crash risk.

    Product
    PETERBILT — PETERBILT 548
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V566000·2026-09-01

    Storyteller Overland Recalls MODE and GXV HILT Vans for Fire Risk

    Storyteller Overland is recalling 2026-2027 MODE and 2026 GXV HILT vans because a rooftop fan component may overheat, increasing the risk of a fire.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV HILT, MODE VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V562000·2026-09-01

    2021-2023 Jeep Grand Cherokee Recall for Rear Coil Spring Defect

    Chrysler is recalling 328,381 Jeep Grand Cherokee vehicles because rear coil springs may detach while driving, increasing crash risk.

    Product
    JEEP — JEEP GRAND CHEROKEE, GRAND CHEROKEE L, GRAND CHEROKEE 4XE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V564000·2026-09-01

    Light Boy Recalls GBX12SK Light Towers Due to Frame Bending Risk

    Light Boy is recalling 2020 and 2023 GBX12SK light towers because the trailer frame may bend, causing the tower to detach and become a road hazard.

    Product
    Light Boy — Light Boy GBX12SK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V559000·2026-09-01

    Jeep Recalls Vehicles Due to Tire Pressure Monitoring System Software Error

    FCA US is recalling specific 2024-2026 Jeep models because a software error may prevent the tire pressure monitoring system from detecting low pressure or illuminating the warning light.

    Product
    JEEP — JEEP WAGONEER L, GRAND CHEROKEE, GRAND WAGONEER L, WAGONEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V565000·2026-09-01

    Forest River Transit Buses Recalled for Wheelchair Lift Control Failure

    Forest River is recalling certain 2024-2025 transit buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS, MOBILITY TRANS SENATOR II, SAFETBUS, GLAVAL UNIVERSAL, STARCRAFT ALLSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V563000·2026-09-01

    Forest River Recalls 2027 Vibe Trailers Due to Carbon Monoxide Risk

    Forest River is recalling 2027 Vibe recreational trailers because the furnace exhaust may not be correctly attached, allowing carbon monoxide to build up inside the cabin.

    Product
    FOREST RIVER — FOREST RIVER VIBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V557000·2026-08-31

    Tiffin Recalls 2026-2027 Wayfarer RVs Due to LP Tank Defects

    Tiffin is recalling 2026-2027 Wayfarer recreational vehicles because the liquid propane tank may lack a remote shut-off or be loose, posing fire and crash risks.

    Product
    TIFFIN — TIFFIN WAYFARER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V555000·2026-08-31

    Jayco Recalls 2027 Entegra Qwest and Melbourne Prestige RVs

    Jayco is recalling certain 2027 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles due to a taillight harness defect that may cause incorrect warning lights on the instrument panel.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE PRESTIGE, QWEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V556000·2026-08-31

    Blue Bird Recalls Vision School Buses Due to Wheelchair Lift Defect

    Blue Bird is recalling 2025-2027 Vision school buses because a faulty electrical contactor may prevent wheelchair lifts from stopping, increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V554000·2026-08-31

    Jayco Recalls 2026-2027 Recreational Vehicles for Incorrect Tire Size Labeling

    Jayco is recalling 2026-2027 Entegra and Seneca recreational vehicles because the tire size on the certification label may be incorrect, which could lead to installing the wrong replacement tires.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE XL, SENECA, SENECA PRESTIGE, ACCOLADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V553000·2026-08-28

    Magic Tilt Watercraft Trailers Recalled Due to Winch Weld Failure

    Magic Tilt is recalling 2025-2026 aluminum watercraft trailers because the winch weld may fail, causing the winch to detach and potentially injure nearby people.

    Product
    MAGIC TILT — MAGIC TILT ALUMINUM WATERCRAFT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide