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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17126–17150 of 39599

  • SevereFDA (Devices)·Z-3004-2018·2018-09-26

    Ventana ultraView Universal Alkaline Phosphatase Red Detection Kit Recalled

    Ventana Medical Systems is recalling 8,211 units of the ultraView Universal Alkaline Phosphatase Red Detection Kit due to leaking and sticking dispensers that may cause false negative IHC results.

    Product
    ultraView Universal Alkaline Phosphatase Red Detection Kit, Catalog Number 05269814001, model 760-501 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2999-2018·2018-09-26

    Ventana Medical Systems Recalls ultraView SISH DNP Detection Kit Due to Leaking

    Ventana Medical Systems is recalling 96 units of the ultraView SISH DNP Detection Kit because leaking and sticking dispensers may cause false negative IHC results.

    Product
    ultraView SISH DNP Detection Kit US, Catalog Number 05572037001, model 760-098 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3007-2018·2018-09-26

    Ventana CONFIRM anti-Estrogen Receptor Antibody Recalled for Dispenser Defects

    Ventana Medical Systems is recalling CONFIRM anti-Estrogen Receptor antibodies due to leaking and sticking dispensers that may cause false negative IHC results.

    Product
    CONFIRM anti-Estrogen Receptor (ER) (SP1) Rabbit Monoclonal Primary Antibody, Catalog Number 05278414001, Model 790-4325 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3002-2018·2018-09-26

    Ventana iVIEW Blue Plus Detection Kit Recalled for Dispenser Leaks

    Ventana Medical Systems is recalling iVIEW Blue Plus Detection Kits because leaking dispensers may cause false negative IHC results.

    Product
    ISH iVIEW Blue Plus Detection Kit, Catalog Number 05266181001, model 760-097 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1968-2018·2018-09-26

    Campomex USA Fresh Cilantro Recalled Due to Cyclospora Contamination

    Campomex USA is recalling fresh cilantro found positive for Cyclospora. The product was distributed in California after being mistakenly released from import hold.

    Product
    Campomex USA fresh cilantro: 5 dozens (60) per box.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2997-2018·2018-09-26

    Ventana ultraView Universal DAB Detection Kit Recalled for Dispenser Defects

    Ventana Medical Systems is recalling ultraView Universal DAB Detection Kits due to leaking and sticking reagent dispensers that may cause false negative IHC results.

    Product
    ultraView Universal DAB Detection Kit, Catalog Number 05269806001, model 760-500 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3013-2018·2018-09-26

    Ventana Medical Systems Recalls Leaking CINtec p16 Histology Reagent Dispensers

    Ventana Medical Systems is recalling 240 units of CINtec p16 Histology reagent dispensers due to leaking and sticking issues that may cause false negative test results.

    Product
    CINtec p16 Histology (250) CE, Catalog Number 06695256001, model 825-4713 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3001-2018·2018-09-26

    Ventana iView DAB Detection Kit Recalled for Leaking and Sticking Dispensers

    Ventana Medical Systems is recalling iView DAB Detection Kits because leaking and sticking dispensers may cause false negative IHC results.

    Product
    iView DAB Detection Kit w/o Secondary Antibody, Catalog Number 05266173001, Model 760-093. For laboratory use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3009-2018·2018-09-26

    Ventana Basal Cell IHC Reagent Recall Due to Dispenser Defects

    Ventana Medical Systems is recalling 75 units of Basal Cell IHC reagents due to leaking and sticking dispensers that may cause false negative results.

    Product
    VENTANA Basal Cell Cktl, (34BE12+p63)250, Catalog Number 06419445001, Model 790-1010 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-3016-2018·2018-09-26

    Ventana ultraView SISH DNP Detection Kit Recalled for Leaking Dispensers

    Ventana Medical Systems is recalling 342 units of the ultraView SISH DNP Detection Kit because leaking dispensers may cause false negative IHC results.

    Product
    ultraView SISH DNP Detection Kit, Catalog Number 05907136001, model 800-098 Immunohistochemistry (IHC) for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·18V666000·2018-09-25

    Kia Recalls 2017-2018 Niro Hybrids for Fire Risk

    Kia is recalling 2017-2018 Niro hybrid vehicles because a faulty relay may overheat the rear seat, increasing the risk of a fire.

    Product
    KIA — KIA NIRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18230·2018-09-25

    Traeger Recalls Scout and Ranger Grills Due to Fire Hazard

    Traeger Grills is recalling Scout and Ranger portable wood pellet grills because grease can leak from the drip tray, posing a fire hazard.

    Product
    Scout and Ranger portable wood pellet grills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V667000·2018-09-25

    Suzuki Recalls 2006 Grand Vitara for Power Steering Belt Tensioner Defect

    Suzuki is recalling 2006 Grand Vitara vehicles because a plastic component in the power steering system can deteriorate, potentially causing a loss of steering assist and increasing crash risk.

    Product
    SUZUKI — SUZUKI GRAND VITARA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V669000·2018-09-25

    Maintainer Service Mechanic Bodies Recalled for Driveshaft Interference Risk

    Maintainer is recalling 2017-2018 Service Mechanic Bodies mounted on Ford F-Series Super Duty trucks because a hydraulic pump may interfere with the front axle driveshaft, potentially causing separation and increasing crash risk.

    Product
    MAINTAINER — MAINTAINER SERVICE/MECHANICBODY FORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V668000·2018-09-25

    Volvo Recalls VNL Trucks Due to Fuel Line Burst Risk

    Volvo is recalling 2016-2019 VNL trucks with Cummins ISX15 engines because a restricted fuel pump cooling circuit screen may cause the fuel line to burst.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V658000·2018-09-24

    Grand Design Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Grand Design is recalling 2019 Reflection, Imagine, and Transcend travel trailers because missing inner axle bearings may cause overheating and fire.

    Product
    GRAND DESIGN — GRAND DESIGN TRANSCEND, REFLECTION, IMAGINE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V655000·2018-09-21

    GM Recalls 2016-2018 Chevrolet Express and GMC Savana for Fire Risk

    General Motors is recalling 2016-2018 Chevrolet Express and GMC Savana vans due to a potential electrical short in the rear climate control module that could cause a headliner fire.

    Product
    CHEVROLET — CHEVROLET, GMC EXPRESS, SAVANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V657000·2018-09-21

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Fuel Line Burst Risk

    PACCAR is recalling 2017-2019 Kenworth and Peterbilt trucks equipped with Cummins ISX15 or X15 diesel engines because a restricted fuel pump cooling circuit screen may cause the fuel line to burst.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T680, W900, T800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V634000·2018-09-21

    Heartland Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Heartland is recalling 2019 travel trailers because missing inner bearing races may cause hub overheating or separation, increasing crash risk.

    Product
    HEARTLAND — HEARTLAND NORTH TRAIL, WILDERNESS, TRAIL RUNNER, MALLARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E092000·2018-09-20

    BMW Recalls TurboCord Portable Chargers Due to Fire and Shock Risk

    BMW is recalling TurboCord Portable Chargers because failing capacitors may cause electrical shock or fire, increasing the risk of injury or death.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V652000·2018-09-20

    BMW Recalls 2018-2019 Models for TurboCord Charger Fire Risk

    BMW is recalling specific 2018-2019 electric and hybrid models because capacitors in the TurboCord Portable Chargers may fail, posing a shock or fire hazard.

    Product
    BMW — BMW 530E, 740LE, X5, I3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E091000·2018-09-20

    Toyota Recalls Scion xB and tC Vehicles with TRD Brake Kits

    Toyota is recalling 2008-2015 Scion xB and 2011-2016 Scion tC vehicles equipped with specific TRD brake kits because the hoses may fail, increasing crash risk.

    Product
    SCION — SCION XB, TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0004-2019·2018-09-19

    Fuzhou Fish Balls Recalled for Undeclared Allergens

    H & C Food Inc. is recalling Fuzhou Fish Balls because they contain undeclared egg, crustacean, and pork.

    Product
    Fuzhou Fish Balls, packaged in a blue and white package bag, in two sizes: Net WT: 14 OZ (400g), UPC: 6 953640 05000 and Net WT:4.5 lbs. (2043g), UPC: 6 953640 050017. Keep Frozen.
    Category
    Food
    Distribution
    1 state