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.

851–875 of 2056

  • 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
  • SevereNHTSA·17V618000·2017-10-04

    Prevost Recalls Motor Coaches Due to Fuel Tank Cradle Defect

    Prevost is recalling 2008-2018 motor coaches because fuel tank cradles may loosen, causing the tank to fall off and increasing crash risk.

    Product
    PREVOST — PREVOST H3-41, X3-45 VIP ENTERTAINER, X3-45 VIP, XL2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E055000·2017-10-02

    IMMI Recalls School Bus Seats Due to Fracturing Buckle Mount Rods

    Indiana Mills and Manufacturing is recalling Generation IV school bus seats because the buckle mount rods may fracture, increasing injury risk in crashes.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17231·2017-09-25

    Delta Recalls J is for Jeep Strollers Due to Fall Hazard

    Delta is recalling about 28,000 J is for Jeep jogging strollers because the leg bracket can break, posing a fall hazard to infants.

    Product
    J is for Jeep brand cross-country all-terrain jogging strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17230·2017-09-21

    Renthal Recalls Gen 1 and Gen 2 Motorcycle Clip-on Handlebars

    Renthal is recalling Gen 1 and Gen 2 motorcycle clip-on handlebars because the clamp can crack and fail, posing a crash hazard. No injuries have been reported.

    Product
    Gen1 and Gen 2 motorcycle clip-on handlebars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3081-2017·2017-09-06

    Alcon Recalls LuxOR Ophthalmic Microscope Floor Stands Due to Caster Defect

    Alcon is recalling 1,074 LuxOR microscope floor stands because casters may break or detach from the base after impact or stress.

    Product
    LX3 Floor Stand for LuxOR Ophthalmic Microscope; Endure LuxOR Q-VUE Ophthalmic Microscope. LX3 Microscope Floor Stands are not stand-alone medical devices, but are used in combination with the LuxOR Ophthalmic Microscope and the LuxOR Ophthalmic Microscope with Q-VUE 3-D Assista
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V494000·2017-08-04

    Trail King Recalls 2012-2014 Gooseneck Trailers Due to Pivot Plate Defect

    Trail King is recalling 2012-2014 gooseneck trailers because a short pivot plate reinforcement may crack, causing the trailer deck to disconnect and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING GOOSENECK TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V482000·2017-07-28

    Chrysler Pacifica Recall: Rear Pinion Bracket Cracking Risk

    Vantage Mobility International is recalling 2017 Chrysler Pacifica lowered floor vehicles because rear pinion brackets may crack, causing wheel wobble and potential loss of control.

    Product
    CHRYSLER — CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E038000·2017-07-18

    TriMark Recalls Ambulance Door Striker Bolts for Crash Safety Non-Compliance

    TriMark is recalling specific door striker bolts used in ambulance door systems because they may fail during a crash, causing doors to open and increasing injury risk.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V452000·2017-07-17

    Daimler Trucks Recalls 2018 Freightliner and Western Star Models for Tow Hook Defect

    Daimler Trucks North America is recalling 2,483 2018 Freightliner and Western Star trucks because their tow hooks may fail during recovery operations, increasing the risk of injury.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR M2 BUSINESS CLASS, 122SD, CASCADIA, 114SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2653-2017·2017-07-05

    Shimadzu Ceiling X-ray Tube Support Recalled for Potential Cracks

    Shimadzu Medical Systems is recalling ceiling-type X-ray tube supports because cracks may develop on the tube holding shaft, posing a risk of equipment failure.

    Product
    SHIMADZU Ceiling Type X-ray Tube Support CH-200/CH-200M Catalog Number: CH-200/CH-200M Holds an x-ray tube unit and collimator combined with an z-ray high voltage generator, radiographic stand, and table. It is designed to perform radiography of patients either in a standing or
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2651-2017·2017-07-05

    Carestream Recalls DRX-Revolution Mobile X-Ray Systems Due to Assembly Defect

    Carestream Health Inc is recalling DRX-Revolution Mobile X-Ray Systems because missing screws could cause the tube and yoke assembly to separate.

    Product
    DRX-Revolution Mobile X-Ray System; MODEL DRXR-1; Catalog # 1019397 (all other countries) and Catalog 1060177 (China only) -- COMMON/USUAL NAME: DRX-Revolution --- The DRX-Revolution is a mobile system used to generate and control X-Rays for diagnostic procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17180·2017-06-20

    Staples Recalls Hazen Mesh Task Chairs Due to Fall Hazard

    Staples is recalling Hazen Mesh Task chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact Staples for a free replacement base.

    Product
    Hazen Mesh Task chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17750·2017-06-16

    Advanced Composites Recalls Bicycle Forks Due to Fall Hazard

    Advanced Composites is recalling about 40 Wound Up Tandem Duo Disc bicycle forks because the fork leg can crack, posing a fall hazard.

    Product
    Bicycle forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2321-2017·2017-06-14

    OrthoPediatrics Recalls Response BandLoc Tensioner Instruments Due to Band Rupture Risk

    OrthoPediatrics Corp is recalling 82 Response BandLoc 5.5/6.0 Tensioner Instruments because over-tensioning can damage the band, causing it to rupture during spine surgery.

    Product
    Response BandLoc 5.5/6.0 Tensioner Instrument The Tensioner Instrument (01-1102-1000) is utilized to allow the surgeon to apply a recommended tension to the band and hold it in place during spine manipulation and set screw tightening.
    Category
    Medical Device
    Distribution
    6 states
  • HighCPSC·17177·2017-06-13

    Noble House Recalls Dining Chairs Due to Leg Breakage and Fall Hazard

    Noble House is recalling about 3,300 dining chairs because the legs can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a free repair kit.

    Product
    Dining chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17175·2017-06-08

    GT Mountain Bicycles Recalled Due to Handlebar Crack Hazard

    Cycling Sports Group is recalling about 1,000 GT mountain bicycles because the handlebars can crack, posing a fall hazard to consumers.

    Product
    GT mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2017·2017-06-07

    Cardinal Digital Bariatric Scales Recalled Due to Seat Failure Risk

    Cardinal Scale Mfg Co is recalling 975 digital bariatric scales because a seat may fail unexpectedly, posing an injury risk.

    Product
    Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V355000·2017-06-01

    Mazda Recalls 2004 RX-8 Vehicles for Front Suspension Control Arm Defect

    Mazda is recalling 2004 RX-8 vehicles because a crack in the front suspension lower control arm ball joint socket may cause the ball joint to separate, potentially leading to loss of steering control.

    Product
    MAZDA — MAZDA RX-8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2163-2017·2017-05-31

    CORPAK CORFLO PEG Kit Recall Due to Potential Connector Breakage

    CORPAK MedSystems is voluntarily recalling CORFLO PEG Kits because the ENFit connector stem may break unexpectedly under stress.

    Product
    CORFLO PEG Kit, Pull 16FR. Product Usage: CORFLO PEG Tubes are intended for delivery of enteral nutrition, water and medications into the stomach. The PEG adapter is the connection point between the tubing and the feeding set/syringe. The adapter is designed as a replaceabl
    Category
    Medical Device
    Distribution
    3 states