The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

33751–33775 of 50502

  • HighFDA (Devices)·Z-0691-2017·2016-12-07

    B. Braun Recalls Sterile IV Start Kits Due to Sterility Testing

    B. Braun Medical is recalling 15,950 Sterile IV Start Kits because non-routine sterility testing returned positive results.

    Product
    Sterile IV Start Kits 50 units/trays per case Convenience kit for IV start procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0679-2017·2016-12-07

    Teleflex Recalls Arrow OnControl Aspiration System Trays Due to Sterility Concerns

    Teleflex Medical is recalling specific lots of Arrow OnControl Ported Aspiration System Trays because the outer sterile package may have an incomplete seal.

    Product
    ARROW OnControl Ported Aspiration System Tray, Sterile, Rx only, The Arrow OnControl Bone Marrow Aspiration System is intended for bone marrow aspiration of the iliac crest of adult and pediatric patients. The Arrow OnControl Bone Marrow Biopsy System is intended for bone marrow…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17044·2016-12-06

    Atrium Recalls SafeHarbor Vinyl Impact Windows Due to Injury Hazard

    Atrium is recalling about 580 SafeHarbor vinyl impact windows because the glass can separate from the frame during hurricanes, posing an impact injury hazard.

    Product
    SafeHarbor vinyl impact windows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17045·2016-12-06

    Target Recalls Acrylic Hanukkah Menorahs Due to Fire Hazard

    Target is recalling clear acrylic Hanukkah menorahs that can melt when candles are burning, posing a fire hazard. Consumers should stop using the products and return them for a refund.

    Product
    Menorahs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16E089000·2016-12-05

    Hickory Springs Recalls Phantomizer 19 Inch Conversion Van Seats

    Hickory Springs is recalling specific Phantomizer 19-inch conversion van seats because the slide tracks may not engage properly, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V875000·2016-12-05

    Ford Recalls 2013-2016 Fusion and 2013-2015 Lincoln MKZ for Seat Belt Defect

    Ford is recalling specific 2013-2016 Fusion and 2013-2015 Lincoln MKZ vehicles because heat from seat belt pretensioners may cause anchor cables to fail, increasing injury risk in a crash.

    Product
    FORD — FORD, LINCOLN FUSION, MKZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V872000·2016-12-05

    Peterbilt Trucks Recalled for Brake Light Switch Defect

    PACCAR is recalling 2017 Peterbilt trucks because brake lights may not illuminate when brakes are applied, increasing crash risk.

    Product
    PETERBILT — PETERBILT 330, 365, 386, 325
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V873000·2016-12-05

    Entegra Recalls 2017 Cornerstone Vans Due to Collision System Defect

    Entegra is recalling 125 2017 Cornerstone vehicles because the collision mitigation system may be installed upside down, reducing its functionality and increasing crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V866000·2016-12-02

    Forest River Recalls 2017 Puma Trailers for Incorrect Federal Tire Placards

    Forest River is recalling 2017 Puma trailers because incorrect Federal placards list wrong tire and rim information, which could lead to under-inflation and increased crash risk.

    Product
    FOREST RIVER — FOREST RIVER PUMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V869000·2016-12-02

    Thor Motor Coach Recalls 2017 Quantum RQ29 Motorhomes for Missing Light

    Thor Motor Coach is recalling 32 model year 2017 Quantum RQ29 motorhomes because they may be missing a required mid-ship marker light, which can increase crash risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V867000·2016-12-02

    Mitsubishi Recalls Outlander Sport Vehicles for Lift Gate Corrosion Risk

    Mitsubishi is recalling 2011-2012 and 2016 Outlander Sport vehicles because the lift gate support tube may corrode, causing the gate to fall suddenly and increase injury risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17717·2016-12-01

    Lexibook Baby Bath Seats Recalled for Drowning Hazard

    CPSC recalls about 7,000 Lexibook baby bath seats and chairs because they can tip over, posing a drowning hazard to babies.

    Product
    Lexibook® Baby Bath Seats and Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17042·2016-12-01

    TCP LED Lamps Recalled for Electrical Shock Hazard

    Technical Consumer Products is recalling about 39,000 LED lamps sold at Habitat for Humanity in California due to an electrical shock hazard.

    Product
    Technical Consumer Products (TCP) LED lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V865000·2016-12-01

    Livin' Lite Recalls 2017 RVs Due to Fire Risk from Gas Line

    Livin' Lite is recalling 2017 Camplight and Quicksilver RVs because a rubber propane gas line can melt and cause a fire. Dealers will replace the line with a copper extension.

    Product
    LIVIN LITE — LIVIN LITE CAMPLIGHT, QUICKSILVER 6.0
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E088000·2016-12-01

    Lippert Brake Axle Recall for Potential Brake Lockup or Failure

    Lippert Components is recalling specific 7000lb and 8000lb Brake Axles because loose flange nuts may cause brakes to lock up or fail to engage, increasing crash risk.

    Product
    SERVICE BRAKES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0512-2017·2016-11-30

    CSM Bakery Recalls 7-Eleven Sugar Cookie Base for Undeclared Peanut

    CSM Bakery Products NA is recalling 7-Eleven Sugar Cookie Base, 50#, because it contains undeclared peanut protein. The product was distributed across 19 states and two territories.

    Product
    7-Eleven Sugar Cookie Base, 50#
    Category
    Food
    Distribution
    19 states
  • HighFDA (Food)·F-0046-2017·2016-11-30

    Enlightened Peanut Butter Ice Cream Recalled for Undeclared Peanuts

    Cedar Crest Specialties is recalling Enlightened Peanut Butter Chocolate Chip Ice Cream because some pints may contain undeclared peanuts due to packaging errors.

    Product
    Enlightened Peanut Butter Chocolate Chip Ice Cream, one pint
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-0635-2017·2016-11-30

    Merit Medical Procedure Kits Recalled for Compromised Sterile Barrier

    Merit Medical Systems is recalling 53 Procedure Kits due to a compromised sterile barrier. The kits were distributed nationwide to specific states and Japan.

    Product
    Procedure Kit. Catalog Numbers K12-04830B and K12-YP030A
    Category
    Medical Device
    Distribution
    Distributed nationwide