The Recall Desk

Hazard

Injury Risk recalls

1,294 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,294
Critical
0
Severe
339
Most recent
2026-09-01

Of the 1,294 injury risk recalls we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 339 (26%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all injury risk recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

176–200 of 1294

  • HighNHTSA·24V284000·2024-04-19

    2024 Tesla Model 3 Side Air Bag Module Missing Deflector

    Tesla is recalling one 2024 Model 3 vehicle. The driver seat side air bag module was assembled without a deflector, which may cause improper deployment and increase the risk of injury during a crash.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1293-2024·2024-03-20

    EasyPoint Needle may detach inside patient during use

    Retractable Technologies is recalling EasyPoint Needles (25G x 5/8", REF: 82091) because the needle cannula may detach from the needle holder inside the patient.

    Product
    EasyPoint Needle, 25G x 5/8", REF: 82091
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E025000·2024-03-14

    Chrysler Recalls Steering Column Modules for Air Bag Deployment Risk

    Chrysler is recalling MOPAR steering column control modules used in 2017-2024 Jeep, Chrysler, and Ram vehicles because improper welding may prevent the driver's air bag from deploying.

    Product
    AIR BAGS:FRONTAL:DRIVER CLOCKSPRING/SPIRAL CASSETTE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V196000·2024-03-14

    Stellantis Recalls 2016 Jeep Wrangler for Air Bag Clockspring Defect

    Stellantis is recalling 2016 right-hand drive Jeep Wranglers because debris may cause the clockspring to fail, preventing the driver's air bag from deploying in a crash.

    Product
    JEEP — JEEP WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1167-2024·2024-02-28

    ESG Cutting Forceps Jaw May Fracture During Use or Inspection

    Olympus Corporation of the Americas is recalling ESG PK Cutting Forceps because the jaw may fracture during pre-procedure inspection or during the procedure, posing a potential injury risk.

    Product
    ESG PK CUTTING FORCEPS, 5MM, 33CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V154000·2024-02-27

    Nissan Rogue and Other Models: Driver Air Bag Inflator Recall

    Nissan is recalling certain 2023-2024 vehicles, including the Rogue, due to a manufacturing issue that may allow the driver's air bag inflator to absorb moisture and deploy improperly.

    Product
    INFINITI — INFINITI, NISSAN QX50, redundant KICKS, VERSA, ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V151000·2024-02-26

    Mercedes-Benz Tourrider Recalled for Potential Roof Hatch Handle Failure

    Daimler Coaches is recalling 2022-2024 Mercedes-Benz Tourrider vehicles because the roof hatch handle may break, potentially delaying emergency exits.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ TOURRIDER BUSINESS, TOURRIDER PREMIUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1056-2024·2024-02-21

    Samsung GM85 Mobile X-ray System Welding Frame Defect Arm Fall Risk

    NeuroLogica is recalling 261 Samsung GM85 mobile x-ray systems due to a welding defect in the moving arm frame that could cause the arm to fall, risking bodily injury.

    Product
    Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E016000·2024-02-14

    Aisin Front Passenger Air Bag Sensor Recall for Unintended Deployment

    Aisin World Corp. of America is recalling certain front passenger air bag weight sensor assemblies that may crack and short circuit, potentially causing unintended deployment or failure to deploy.

    Product
    AIR BAGS:SENSOR:OCCUPANT CLASSIFICATION:FRONT PASSENGER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V096000·2024-02-09

    Bugatti Recalls Chiron Vehicles for Seat Belt Chime Defect

    Bugatti is recalling 2016-2023 Chiron vehicles because the seat belt warning chime may not activate. This defect increases the risk of injury during a crash.

    Product
    BUGATTI — BUGATTI CHIRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V099000·2024-02-09

    Ford Recalls 2018-2020 Expedition and Navigator for Seat Belt Defect

    Ford is recalling 2018-2020 Expedition and Lincoln Navigator vehicles because the seat belt pretensioner may deploy and lock, preventing the belt from retracting or extending.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E009000·2024-02-08

    GM Recalls Autoliv Driver Front Air Bags for 2011-2012 Chevrolet Models

    General Motors is recalling Autoliv driver front air bags sold as service replacement parts for 2011-2012 Chevrolet Silverado 1500, Suburban, and Tahoe vehicles due to a manufacturing defect.

    Product
    AIR BAGS:FRONTAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0972-2024·2024-02-07

    NovoTHOR Whole Body Light Pod Gen 3.0 Canopy Strut Ball Stud May Fail

    A ball stud on the gas strut may fail on NovoTHOR Whole Body Light Pod units, potentially causing injury if the canopy malfunctions while someone is using the device.

    Product
    NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Devices)·Z-0781-2024·2024-01-31

    Medical X-Ray System Recall Due to Parts Falling Off

    Sedecal SA is recalling 845 Sedecal X Optima URS diagnostic x-ray systems after parts fell off the equipment, creating a safety risk to patients and users. The affected units were distributed in Alabama, Florida, and North Carolina.

    Product
    Sedecal X Optima URS digital mobile diagnostic x-ray system. A a stationary x-ray unit with a universal swivel arm. It allows one to take exposures of patients in standing, sitting, or laying position.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0757-2024·2024-01-24

    Maquet PowerLEDII Operating Room Light System Recalled for Fall Risk

    Getinge Usa Sales Inc is recalling Maquet PowerLEDII OR light systems due to a potential for the light to fall in the operating room. No injuries have been reported.

    Product
    Maquet PowerLEDII OR Light System, Model Names and Catalog Numbers PWDII77SF - ARDPWT629100A, PWDII555DF - ARDPWT629101A, PWDII555SF - ARDPWT629102A, PWDII755DF - ARDPWT629103A, PWDII755SF - ARDPWT629104A, PWDII775DF - ARDPWT629105A, PWDII775SF - ARDPWT629106A, PWDII50DF - ARDPWT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0762-2024·2024-01-24

    Maquet Orchide OR Light Systems recalled due to fall risk

    Getinge USA is recalling Maquet Orchide OR Light Systems due to a potential for light fixtures to fall in the operating room. No injuries have been reported.

    Product
    Maquet Orchide OR Light Systems, Model Numbers and Catalog Numbers OHDII FHD QL VP01 - ARD568803935, OHDII FHD QL AIR03 U - ARD568803952, OHDII FHD QL AIR03 E - ARD568803967, OHDII FHD QL AIR04 E/U - ARD568803968, OHDII FHD QL+ VP01 - ARD569204944, OHDII AIR03 QL FHD E - ARD56880
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0713-2024·2024-01-17

    Wheelchair Control Device Throttle Lever May Stick During Operation

    The Scoot Control R-net wheelchair attendant controller's throttle lever may stick and fail to return to neutral, potentially causing unwanted chair movement. A total of 129 units were distributed in Tennessee and Texas.

    Product
    Scoot Control R-net, Product Number P015-61. The Scoot Control is intended to support a wheelchair attendant in controlling or maneuvering a power chair
    Category
    Medical Device
    Distribution
    2 states
  • HighNHTSA·24V019000·2024-01-17

    Newmar motorhomes recalled for improperly welded seat mounting plates

    Newmar is recalling certain 2016–2023 motorhomes because seat pedestal mounting plates may be improperly welded, risking seat loosening or detachment and increasing injury risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE, DUTCH STAR, ESSEX, MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide