The Recall Desk

Hazard

Structural Defect recalls

2,112 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,112
Critical
3
Severe
1,155
Most recent
2026-10-20

Of the 2,112 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 1,155 (55%) 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.

626–650 of 2112

  • SevereNHTSA·21V194000·2021-03-19

    Isuzu and Chevrolet Trucks Recalled for Rear Axle U-Bolt Nut Defect

    Isuzu is recalling 2015-2021 Isuzu, Chevrolet, and International trucks because rear axle U-bolt nuts may loosen, causing axle misalignment and potential loss of power.

    Product
    CHEVROLET — CHEVROLET, INTERNATIONAL MOTORS, ISUZU 5500HD, 4500XD, CHEVY 5500HD, CHEVY 4500HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V197000·2021-03-19

    Mercedes-Benz Recalls Vehicles with Potential Front Roof Panel Bonding Defect

    Mercedes-Benz is recalling specific 2014-2020 models equipped with panoramic sunroofs because the front roof panel may not have been bonded correctly during a prior repair.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300, S 450, C 350 E, CLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1201-2021·2021-03-17

    Medtronic Recalls Valiant Navion Thoracic Stent Grafts Due to Structural Defects

    Medtronic is recalling 33,430 Valiant Navion Thoracic Stent Graft Systems worldwide due to endoleaks, stent fractures, and ring enlargement.

    Product
    Valiant Navion Thoracic Stent Graft System. For endovascular repair of lesions in the descending thoracic aorta (DTA).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1186-2021·2021-03-17

    Stryker Recalls Triathlon Knee Baseplates Due to Manufacturing Defect

    Stryker is recalling 11 Triathlon Tritanium Tibial Baseplates because a manufacturing defect may prevent the knee insert from locking securely.

    Product
    Prosthesis, knee, patello/femorotibial, semi-constrained, uncemented, porous, coated, polymer/metal/polymer.
    Category
    Medical Device
    Distribution
    13 states
  • HighNHTSA·21V171000·2021-03-12

    ATC Recalls 2018-2021 ARV Trailers Due to Insufficient Safety Chains

    ATC is recalling 2018-2021 ARV Gamechanger and Pro Bumper Pull trailers because the installed safety chains are rated lower than the trailer's axle capacity, posing a crash risk.

    Product
    ATC ARV — ATC ARV PRO BUMPER PULL, GAMECHANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V140000·2021-03-05

    Ford Recalls 2021 Mustang Mach-E for Loose Front Subframe Bolts

    Ford is recalling 2021 Mustang Mach-E vehicles because front subframe bolts may not have been tightened properly, which could reduce crash performance and increase injury risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V119000·2021-02-25

    Vermeer Recalls 2021 BC900XL Trailers Due to Axle Bolt Issue

    Vermeer is recalling 2021 BC900XL brush chipper trailers because axle mounting bolts may not be tightened properly, increasing crash risk.

    Product
    VERMEER — VERMEER BC900XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V107000·2021-02-24

    Lamborghini Recalls Aventador SVJ Vehicles Due to Hood Hinge Defect

    Lamborghini is recalling 2018-2021 Aventador SVJ vehicles because hood hinge screws may loosen, potentially causing the hood to detach at high speeds.

    Product
    LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V106000·2021-02-23

    Mercedes-Benz Metris Recall for Improperly Welded Front Passenger Seat Frame

    Daimler Vans USA is recalling 2021 Mercedes-Benz Metris vans because the front passenger seat frame base may not have been welded properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V097000·2021-02-19

    KME Predator Fire Trucks Recalled for Insufficient Rear Axle Welds

    KME is recalling certain Predator fire trucks because rear axle welds may be insufficient, potentially causing loss of vehicle control and increasing crash risk.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR RESCUE, PREDATOR PANTHER PUMPER, PREDATOR SS PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V090000·2021-02-18

    Ford F-Series Trucks Recalled for Potential Windshield Detachment in Crashes

    Ford is recalling certain 2020-2021 F-150 and Super Duty trucks because the windshield may not be properly bonded, risking detachment in a crash. Dealers will remove and reinstall the windshield at no cost.

    Product
    FORD — FORD F-450 SD, F-350 SD, F-250 SD, F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1090-2021·2021-02-17

    Cardinal Health Recalls Lab Coats and Gowns Due to Defects

    Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential rips, holes, and foreign material.

    Product
    Lab Coats SMS X-Large Blue, SKU 2203LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E012000·2021-02-16

    Reyco Granning Recalls Fire Truck Independent Front Suspensions

    Reyco Granning is recalling fire truck independent front suspensions because steering gear mounting bolts may loosen, potentially causing steering difficulties or loss of control.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0925-2021·2021-02-10

    Hill-Rom Liko Multirall 200 Overhead Lifts Recalled for Detachment Risk

    Hill-Rom is recalling Liko Multirall 200 overhead lifts because a strap lock may not fully engage, causing the lift to detach from the rail and potentially drop the patient.

    Product
    Liko Multirall 200 overhead lift- overhead lift is a general-purpose lift with the intended use in healthcare, intensive care and rehabilitation. Affected devices: Liko Multirall 200 (product number 3130001) Universal SlingBar 450 R2R (product number 3156095) Universal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V057000·2021-02-05

    Mercedes-Benz Recalls GLE and GLS Models for Dashboard Defect

    Mercedes-Benz is recalling 2020-2021 GLE and GLS models because the dashboard may not be properly secured, which could impair airbag inflation in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350, GLE 450, GLS 450, AMG GLE53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E005000·2021-01-25

    Brembo Brake Pads Recalled for Potential Friction Material Detachment

    Brembo is recalling specific brake pads that may corrode and detach, potentially increasing stopping distance and crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:PADS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0853-2021·2021-01-20

    GE Healthcare Recalls NM/CT 850 Systems Due to Loose Rotor Bearing Screws

    GE Healthcare is recalling 24 NM/CT 850 systems because loose rotor bearing screws caused a bearing to release in one field unit.

    Product
    GE NM/CT 850 system Model Number H3907AD - Product Usage: intended for general Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0805-2021·2021-01-20

    Siemens Uroskop Omnia X-ray System Recalled for Support Arm Risk

    Siemens is recalling six Uroskop Omnia X-ray systems because the monitor support arm may become dislodged after intense, long-term use.

    Product
    Uroskop Omnia, Model no. 10094910 - Product Usage: a solid state detector fluoroscopic X-ray system, primarily for urological applications (functional x-ray diagnosis, endourology and minimal invasive urology/surgery).
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0654-2021·2020-12-30

    Nova Ortho-Med Recalls Star 8 Rolling Walkers Due to Fork Detachment Risk

    Nova Ortho-Med is recalling Star 8 Rolling Walkers because the front fork may unscrew from the leg, creating instability and a risk of the fork falling off.

    Product
    Star 8 Rolling Walker/Rollator, Items: 4258/ BK(Black)/ BL(Blue)/ DB(Sky Blue)/ PL(Purple)/ RD(Red)
    Category
    Medical Device
    Distribution
    38 states
  • SevereNHTSA·20V764000·2020-12-21

    GM Recalls 2010-2013 Buick and Chevrolet Models for Rear Suspension Defect

    General Motors is recalling specific Buick and Chevrolet vehicles because excessive corrosion protection on rear toe links may cause them to fracture, increasing crash risk.

    Product
    BUICK — BUICK, CHEVROLET LACROSSE, REGAL, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V786000·2020-12-16

    Audi Recalls 2020 Q3 Vehicles Due to Brake Pedal Plate Defect

    Volkswagen Group of America is recalling 2020 Audi Q3 vehicles because the brake pedal plate can bend or detach, increasing crash risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide