The Recall Desk

Hazard

Structural Defect recalls

2,094 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,094
Critical
3
Severe
1,081
Most recent
2026-09-02

Of the 2,094 structural defect recalls we have scored against our rubric, 3 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,081 (52%) 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 structural defect 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.

276–300 of 2094

  • HighFDA (Devices)·Z-1555-2024·2024-04-24

    Philips Achieva 3.0TX PET-MRI Patient Support Table Installation Defect

    Philips is recalling the Achieva 3.0TX PET-MRI system because the patient support table floor plate may be incorrectly installed.

    Product
    Achieva 3.0TX for PET, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1552-2024·2024-04-24

    Philips Achieva 1.5T MRI System: Patient Support Table Floor Plate Installation Issue

    Philips is recalling 69 units of the Achieva 1.5T Initial MRI system due to potential issues with the patient support table floor plate installation, which may affect patient safety during imaging.

    Product
    Achieva 1.5T Initial, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1575-2024·2024-04-24

    Philips MRI Patient Support Table Floor Plate May Be Incorrectly Installed

    Philips is recalling 347 Intera 1.5T MRI systems worldwide because the patient support table floor plate may be incorrectly installed, potentially compromising patient support stability during use.

    Product
    Intera 1.5T, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1550-2024·2024-04-24

    Philips Achieva 1.5T MRI Systems Recalled Due to Incorrect Support Table Installation

    Philips is recalling 1,921 Achieva 1.5T MRI systems worldwide because the patient support table floor plate may be incorrectly installed. Healthcare facilities should verify proper installation.

    Product
    Achieva 1.5T, Magnetic Resonance System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V287000·2024-04-23

    Kia Sorento power steering wiring harnesses may be incorrectly assembled

    Kia is recalling certain 2024 Sorento vehicles because the motor driven power steering wiring harness may be incorrectly assembled, which can result in a loss of power steering assist.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V263000·2024-04-11

    Keystone Recalls 2024 Trailers Due to Axle Frame Contact Risk

    Keystone RV is recalling 214 specific 2024 trailer models because the suspension equalizer may allow the axle to contact the frame, increasing crash risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN HAMPTON, RETREAT, ASPEN TRAIL LOFT, RESIDENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1462-2024·2024-04-10

    Mobile X-ray System Structural Cable Defect Affects Safety Function

    Agfa DX-D 100 mobile X-ray systems have a structural cable defect in the support column that may prevent the safety mechanism from blocking the arm if the cable fails, potentially resulting in patient injury.

    Product
    Agfa DX-D 100 system-Digital Radiography mobile X-ray System. A mobile X-Ray modality, consisting of X-Ray console, generator, tube, digital detector, and workstation. This modality is used to generate projection X-Ray images of human patients. Models: 5411/ 050, A5411/ 0300
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1395-2024·2024-04-03

    Emergency traction splint adhesive failure may compromise device function

    Emergency Products & Research is recalling 190,000 O.T.D. traction splints because adhesive may fail to secure the pole insert, potentially compromising function in emergency medical situations.

    Product
    O.T.D - Optimum Traction Device - Street Orange. Single use traction splint.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V233000·2024-03-27

    2025 Peterbilt and Kenworth Trucks Recalled Over Steering Gear Defect

    PACCAR is recalling certain 2025 Peterbilt and Kenworth trucks because the steering gear sector shaft may have been improperly heat-treated, which can cause the gear teeth to crack or fracture.

    Product
    PETERBILT — PETERBILT, KENWORTH 579, T680, T280, T380
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V223000·2024-03-22

    Ford Maverick and Bronco Sport tires may have been manufactured incorrectly

    Ford is recalling certain 2023 Maverick and Bronco Sport vehicles because the tires may have been manufactured incorrectly, which may result in a loss of vehicle handling and control.

    Product
    FORD — FORD MAVERICK, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V214000·2024-03-20

    Kia Telluride driveshafts may not fully engage, allowing roll away

    Kia is recalling certain 2020-2024 Telluride vehicles because the intermediate shaft and right front driveshaft may not be fully engaged, which can result in roll away while in PARK.

    Product
    KIA — KIA TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V216000·2024-03-20

    LiveWire rear axle and shock joint nuts may not be tightened

    LiveWire is recalling certain 2024 S2 Del Mar motorcycles because the rear axle and lower shock joint nuts may not have been properly tightened. 165 units are affected.

    Product
    LIVEWIRE — LIVEWIRE S2 DEL MAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1213-2024·2024-03-06

    Colonoscope Model PCF-HQ190L Recalled for Missing Protective Adhesive

    Olympus is recalling 28 colonoscopes (Model PCF-HQ190L) due to missing adhesive that protects the device from vibration, temperature changes, and physical shock. The defect could cause device malfunction during procedures.

    Product
    Colonoscope, Model Number PCF-HQ190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1211-2024·2024-03-06

    Colonoscope Model PCF-H190L Recalled for Missing Protective Adhesive

    Olympus Corporation recalled 31 colonoscopes lacking a protective adhesive that shields against vibration, temperature fluctuations, and shock. The missing adhesive may affect device structural integrity under physical stress.

    Product
    Colonoscope, Model Number PCF-H190L.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2024·2024-03-06

    Colonoscope Model CF-H180AL Recalled Due to Missing Protective Adhesive

    Olympus is recalling 36 colonoscopes with specific serial numbers that lack a protective adhesive, risking device failure if exposed to vibration, temperature changes, or shock loads.

    Product
    Colonoscope, Model Number CF-H180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1208-2024·2024-03-06

    Colonoscope Model CF-Q180AL Recalled Due to Missing Protective Adhesive

    Olympus is recalling two colonoscopes (Model CF-Q180AL, serial numbers 2602060 and 2603763) due to missing protective adhesive that normally guards against vibration, temperature changes, and shock loads.

    Product
    Colonoscope, Model Number CF-Q180AL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1210-2024·2024-03-06

    Olympus Colonoscope Recall: Missing Protective Adhesive in 47 Units

    Olympus is recalling 47 colonoscope units (Model PCF-H190DL) because they were assembled without protective adhesive. The missing adhesive may cause equipment failure under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number PCF-H190DL.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1206-2024·2024-03-06

    Colonoscope Model CF-HQ190I recalled for missing protective adhesive

    Olympus is recalling certain repaired Model CF-HQ190I colonoscopes assembled without protective adhesive, which may cause equipment failure under vibration, temperature changes, or shock.

    Product
    Colonoscope, Model Number CF-HQ190I.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V163000·2024-02-29

    Land Rover Recalls 2024 Discovery Sport for A-Pillar Bolt Issue

    Land Rover is recalling 2024 Discovery Sport vehicles because a lower A-pillar bolt may be improperly fastened, reducing structural strength and increasing injury risk in a crash.

    Product
    LAND ROVER — LAND ROVER DISCOVERY SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V143000·2024-02-23

    Ford F-650 and F-750 parking brake levers may release unexpectedly

    Ford is recalling certain 2023-2024 F-650 and F-750 vehicles because the parking brake may malfunction and allow the lever to be released without pressing the release button.

    Product
    FORD — FORD F-650 SD, F-650 INCOMPLETE CHASSIS, F-750 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V145000·2024-02-23

    Kenworth trucks fitted with air tanks holding insufficient brake air

    PACCAR is recalling certain 2009-2024 Kenworth trucks because the air tanks have an insufficient volume of air for the brake system, which can reduce braking performance.

    Product
    KENWORTH — KENWORTH T370, T800, W900, T440
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V131000·2024-02-22

    Jeep Grand Cherokee steering knuckles may separate at the ball joint

    Chrysler is recalling certain 2024 Jeep Grand Cherokee vehicles because an improperly machined steering knuckle may separate, causing the wheel to fall outward. 250 units affected.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V132000·2024-02-22

    Jeep Grand Cherokee upper control arm ball joints may separate

    Chrysler is recalling certain 2021-2023 Jeep Grand Cherokee L and 2022-2023 Grand Cherokee vehicles because the upper control arm ball joint and steering knuckle may separate. 338,238 units affected.

    Product
    JEEP — JEEP GRAND CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide