The Recall Desk

Hazard

Structural Failure recalls

2,056 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,056
Critical
10
Severe
1,049
Most recent
2026-09-17

Of the 2,056 structural failure recalls we have scored against our rubric, 10 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (51%) are Severe.

Which agencies issued them

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all structural failure 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.

826–850 of 2056

  • SevereNHTSA·18V118000·2018-02-17

    Hyundai Recalls 2018 Santa Fe Vehicles Due to Steering Wheel Defect

    Hyundai is recalling 2018 Santa Fe and Santa Fe Sport vehicles because the steering wheel assembly may break and separate from the column while driving.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E006000·2018-01-24

    Dainese Recalls AGV Carbon Modular Helmets Due to Chin Bar Defect

    Dainese is recalling 325 AGV Carbon Modular motorcycle helmets because glue may have caused the chin base material to deteriorate, increasing injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18E005000·2018-01-24

    Fuel Helmets Recalling Specific Models Due to Strap Failure Risk

    Fuel Helmets is recalling specific models because the securing strap may fail in extreme temperatures, increasing injury risk in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0331-2018·2018-01-17

    Philips Brilliance iCT CT Scanner Recall Due to Potential Gantry Screw Failure

    Philips is recalling 702 Brilliance iCT computed tomography systems because screws holding an internal gantry component may come loose, potentially causing noise.

    Product
    Philips Healthcare Brilliance iCT computed tomography x-ray system
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0333-2018·2018-01-17

    Philips IQon Spectral CT Scanner Recall Due to Potential Gantry Screw Failure

    Philips is recalling IQon Spectral CT systems because screws holding the internal gantry to the main bearing may come loose, potentially causing noise.

    Product
    Philips Healthcare IQon Spectral CT computed tomography x-ray system
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·18V006000·2018-01-04

    Altec Recalls 2010-2011 Knuckle Boom Cranes Due to Bearing Fastener Failure

    Altec Industries is recalling 2010-2011 Effer 440 and 470 Knuckle Boom Cranes because rotation bearing fasteners may fail, causing the pedestal to crack and increasing injury risk.

    Product
    ALTEC — ALTEC 470 KNUCKLE BOOM CRANE, EFFER 440
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18071·2017-12-22

    Vilo Home Recalls Marseille Dining Benches Due to Fall Hazard

    Vilo Home is recalling Marseille dining benches because the foam seat cushion and base can crack, causing the bench to collapse and posing a fall hazard.

    Product
    Marseille dining benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0232-2018·2017-12-20

    Fujifilm FDR Visionary Suite X-ray Tube Recall for Cracking Risk

    Fujifilm is recalling three FDR Visionary Suite systems because cracks may develop in the X-ray tube holding shaft, posing a potential safety issue.

    Product
    FUJIFILM FDR Visionary Suite with CH-200. Model # CH-200, Catalog: Visionary Suite (FMSU Marketing Name) The FDR Visionary Suite is intended to generate digital or conventional radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts o
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0193-2018·2017-12-13

    Pro-Med Instruments Recalls DORO Sterile Disposable Skull Pins Due to Breakage

    Pro-Med Instruments is recalling DORO Sterile Disposable Skull Pins because two instances of pin tip breakage were reported during surgery.

    Product
    pmi, pro med instruments, DORO(R) Sterile Disposable Skull Pins, 3 pieces (3 pieces per blister, 12 blisters per box), STERILE R, Rx ONLY The DORO(R) Skull Pins are inserted into the receptacles of the skull clamp and fixate the head during surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V785000·2017-12-08

    KZRV Recalls 2014-2015 Durango Gold Trailers Due to Step Rivet Failure

    KZRV is recalling 2014-2015 Durango Gold recreational trailers because quad entry step rivets may shear, causing steps to fail and increasing the risk of falls and injury.

    Product
    KZRV — KZRV DURANGO GOLD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·18044·2017-11-21

    Plycem Recalls Allura Decking Due to Fall and Injury Hazards

    Plycem is recalling Allura fiber cement decking and fascia because the materials can crack, causing consumers to fall through and suffer injuries.

    Product
    Allura decking
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0068-2018·2017-11-15

    Lima Delta Cup Beater Positioner Recalled for Potential Welding Defects

    Lima is recalling 20 Delta Cup Beater Positioner units in the US due to suboptimal welding that may reduce mechanical strength and cause breakage during use.

    Product
    Delta Cup Beater  Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·17V709000·2017-11-13

    Altec Recalls Aerial Cable Placers Due to Boom Tip Crack Risk

    Altec Industries is recalling 1992-2000 Aerial Cable Placer AP45 vehicles because boom tips may crack and fail, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL CABLE PLACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V706000·2017-11-09

    Honda Recalls 2017 Civic Vehicles Due to Drivetrain Defect

    Honda is recalling 2017 Civic Sedans and Coupes because a defective halfshaft may break, potentially causing the vehicle to roll away and increasing crash risk.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0059-2018·2017-11-08

    Teleflex Percuvance Percutaneous Surgical System Recalled for Tool Tip Breakage

    Teleflex is recalling specific Percuvance surgical instruments because the tool tip jaws may break, causing fragments to fall off during use.

    Product
    Teleflex(R) Percuvance(TM) Percutaneous Surgical System, Components: (a) 5 mm Atraumatic Johans Grasper, Catalog Number PCVJG5 (b) 5 mm Maryland Dissector, Catalog Number PCVMD5 (c) 5 mm Hem-o-lok Clip Applier, Catalog Number PCVHCA5 (d) 5 mm Traumatic Gripper Grasper, Catalo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0013-2018·2017-10-18

    Handicare A-Series Patient Lifts Recalled for Premature Strap Wear

    Handicare is recalling 8 A-Series patient lifts because the lift straps may wear prematurely at maximum load, posing a risk of patient drop.

    Product
    PRISM MEDICAL A-625, MAX. LOAD 625 lbs. 283 Kgs., Patient lift, non-A/C powered
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·17V637000·2017-10-11

    Nissan Recalls 2012 Versa Hatchbacks for Front Coil Spring Fracture Risk

    Nissan is recalling 2012 Versa Hatchbacks sold in 23 states and D.C. because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.

    Product
    NISSAN — NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0005-2018·2017-10-11

    Permobil Recalls Electric Wheelchairs Due to Top Plate Assembly Failure Risk

    Permobil is recalling 5,539 Corpus II electric wheelchairs because the top plate assembly may fail, potentially disconnecting the seating system from the base.

    Product
    Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR
    Category
    Medical Device
    Distribution
    Distributed nationwide