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.

38126–38150 of 50506

  • HighNHTSA·15V467000·2015-07-27

    Dodge Charger Recall for Overly Sensitive Side Impact Sensors

    Chrysler is recalling 2011-2014 Dodge Chargers because overly sensitive side impact sensors may cause air bags to deploy unexpectedly, increasing crash risk.

    Product
    DODGE — DODGE CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V463000·2015-07-24

    General Motors Recalls 2013-2016 Cadillac ATS for Sunroof Defect

    General Motors is recalling 2013-2016 Cadillac ATS vehicles because the sunroof may close automatically if the switch is pressed inadvertently, posing a risk of personal injury.

    Product
    CADILLAC — CADILLAC ATS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V464000·2015-07-24

    Ford Recalls 2015-2016 Vehicles Due to Parking Brake Defect

    Ford is recalling specific 2015-2016 models because the parking brake may not fully engage, increasing the risk of the vehicle rolling away on a slope.

    Product
    FORD — FORD, LINCOLN EXPLORER, MKT, MKS, FLEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15195·2015-07-23

    Husqvarna Recalls Lawn Tillers Due to Unintended Movement Risk

    Husqvarna is recalling approximately 24,000 Ariens, Husqvarna, Jonsered, and Poulan Pro tillers because the transmission shift rod can cause the machine to move unintentionally, posing a risk of injury.

    Product
    Lawn and garden tillers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15196·2015-07-23

    UPPAbaby Recalls 2015 Strollers and RumbleSeats Due to Choking Hazard

    UPPAbaby is recalling 2015 CRUZ and VISTA strollers and RumbleSeats because the foam bumper bar can break off, posing a choking hazard to children.

    Product
    UPPAbaby 2015 CRUZ, 2015 VISTA strollers and 2015 RumbleSeat
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15197·2015-07-23

    Briggs & Stratton Recalls Simplicity Riding Mowers Due to Projectile Risk

    Briggs & Stratton is recalling about 2,800 Simplicity riding mowers and garden tractors because the chute deflector can fail, posing a risk of injury from projectiles.

    Product
    Briggs & Stratton Simplicity Riding Mowers, Garden Tractors and Mower Decks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V461000·2015-07-23

    Chrysler Recalls 2013-2015 Vehicles for Radio Software Vulnerability

    Chrysler is recalling specific 2013-2015 Ram, Jeep, Dodge, and Chrysler vehicles because radio software vulnerabilities allow unauthorized remote access to vehicle control systems, increasing crash risk.

    Product
    RAM — RAM, DODGE, JEEP 4500, VIPER, 5500, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15743·2015-07-23

    Polaris Recalls Youth RZR Vehicles Due to Fuel Pump Fire Hazard

    Polaris is recalling about 4,300 Youth RZR 170 EFI vehicles because a fuel pump retaining ring can leak, posing a fire hazard.

    Product
    Polaris Youth RZR recreational off-highway vehicle
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2094-2015·2015-07-22

    Breas Vivo 50 Home Care Ventilator Recalled for Keypad Malfunction

    Breas Medical AB is recalling 846 Vivo 50 Home Care Ventilators because a keypad malfunction can cause the device to stop treatment without an alarm.

    Product
    Breas Vivo 50 Home Care Ventilator Product Usage: Respiratory Care
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2064-2015·2015-07-22

    Omnilife Apex ARC Hip Stem Recalled for Sterile Pouch Breach Risk

    Omnilife Science Inc. is recalling 146 Apex ARC Hip Stems because the sterile packaging may breach during shipping or handling.

    Product
    Apex ARC Hip Stem, HA Coated, Size 5; Product Code: HC-21005-HA Product Usage: The Apex ARC Hip Stem is the femoral component of a primary or revision total hip replacement. This femoral hip stem is intended for press-fit application and is provided sterile for single use.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V456000·2015-07-22

    Peterbilt Trucks Recalled for Alternator Cable Chafing Fire Risk

    PACCAR is recalling 2012-2016 Peterbilt trucks because alternator cables may chafe against a metal line, creating a fire risk.

    Product
    PETERBILT — PETERBILT 365, 587, 386, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2846-2015·2015-07-22

    Project 7 Recalls Sour Caramel Apple Chewing Gum for Undeclared Milk

    Project 7 is recalling Sour Caramel Apple Chewing Gum because the caramel flavoring contains undeclared milk, posing a risk to individuals with milk allergies.

    Product
    Sour Caramel Apple Chewing, net wt .53 oz, Gum UPC 844911 002919. Sour Caramel Apple chewing gum tablet packed in 12ct metalized PET Pouch with zipper.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2077-2015·2015-07-22

    Sorin Stockert Heater-Cooler 3T Recalled for Potential Organism Colonization

    Sorin Group USA is recalling 21 Sorin Stockert Heater-Cooler 3T units due to the potential for organism colonization, including Mycobacteria, if proper disinfection and maintenance are not performed.

    Product
    Sorin Stockert Heater-Cooler 3T, 240 V / 60 Hz Temperature control for extracorporeal perfusion of durations up to 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2081-2015·2015-07-22

    Sorin Stockert Heater-Cooler 3T Recalled for Potential Organism Colonization

    Sorin Group USA is recalling 131 Stockert Heater-Cooler 3T units due to potential colonization of organisms, including Mycobacteria, if proper disinfection and maintenance are not performed.

    Product
    Sorin Stockert Heater-Cooler 3T, 200 V / 50Hz / 60 Hz Temperature control for extracorporeal perfusion of durations up to 6 hours.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2072-2015·2015-07-22

    Biomet Recalls A.L.P.S. Medium Bone Plate Forceps Due to Assembly Error

    Biomet is recalling 223 units of A.L.P.S. Medium Bone Plate Forceps because they were assembled with incorrect grip arm tips, potentially preventing surgeons from clamping plates to bone.

    Product
    A.L.P.S. - Medium Bone Plate Forceps. Orthopedic manual surgical instrument.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-2083-2015·2015-07-22

    Maquet Recalls FLOW-i Anesthesia System Modules Due to Suction Failure

    Maquet is recalling 104 FLOW-i Anesthesia System Auxiliary O2 and Suction Modules because the suction function may not activate or be controlled by the switch.

    Product
    The FLOW-i Anesthesia System Axillary O2 and Suction Module, Device Part number: 66 79 847 FLOW-i Anesthesia System: Is indicated for administering inhalation anesthesia while controlling the entire ventilation of patients with no ability to breathe, as well as in supporting…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2089-2015·2015-07-22

    Eizo RadiForce RX850 Medical Monitors Recalled for Display Abnormalities

    Eizo is recalling RadiForce RX850 medical monitors because they may display images abnormally when connected to specific graphics boards using DisplayPort.

    Product
    RadiForce RX850, 8MP Color LCD Monitor, Part Code No. 0FTD1958A2, UPC 690592037180. This product is intended to be used in displaying and viewing digital images those of digital mammography for review and analysis by trained medical practitioners.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V459000·2015-07-22

    Chrysler Recalls Ram Trucks Due to Air Bag Wiring Harness Defect

    Chrysler is recalling 2012-2014 Ram trucks because a steering wheel wiring harness may rub against the air bag retainer, potentially causing unexpected air bag deployment.

    Product
    DODGE — DODGE, RAM RAM 5500, 4500, RAM 4500, RAM 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2058-2015·2015-07-22

    Biomet Recalls 50 A.L.P.S. Cortical Locking Screws Due to Packaging Defect

    Biomet, Inc. is recalling 50 A.L.P.S. 3.5mm x 60 mm Cortical Locking Screws because the sterile packaging was not sealed, posing a risk of infection.

    Product
    A.L.P.S., 3.5mm x 60 mm Cortical Locking Screw. Bone fixation screw
    Category
    Medical Device
    Distribution
    0 states