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.

276–300 of 2056

  • HighFDA (Devices)·Z-1470-2023·2023-05-03

    Digital X-ray System Arm May Break, Posing Injury Risk

    FUJIFILM's FDR AQRO digital X-ray system arm may break during use. The tube head support is susceptible to failure, which could cause serious harm to patients or operators.

    Product
    FujiFilm FDR AQRO (Model DR-XD1000)- A digital mobile X-ray system intended for use in general purpose radiography for generating radiographic images of human anatomy, including adult, pediatric, and neonatal exams
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1403-2023·2023-04-26

    FDA Recalls MectaLIF ANTERIOR Interbody Fusion Device Due to Screw Breakage Risk

    Medacta Usa Inc is recalling the MectaLIF ANTERIOR interbody fusion device due to potential breakage of the small screw that affixes the anti-backout plate. The recall affects 34 units distributed in the United States.

    Product
    MectaLIF ANTERIOR - Lag Plate Flush H16, REF 03.30.303, interbody fusion device
    Category
    Medical Device
    Distribution
    5 states
  • HighNHTSA·23V279000·2023-04-19

    Triple E RV Recalls 2020-2023 Wonder Motorhomes for Bed Bracket Defect

    Triple E RV is recalling 2020-2023 Wonder W24RTB motorhomes because an incorrectly installed bed stay bracket may fail, causing the bed lid to fall and increasing injury risk.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V270000·2023-04-14

    Winnebago Micro Minnie spare tire carrier failure and detachment risk

    Winnebago is recalling 2021–2023 Micro Minnie travel trailers because the spare tire carrier may fail and detach, posing a road hazard and increasing crash risk. Dealers will replace the carrier free of charge.

    Product
    WINNEBAGO — WINNEBAGO MICRO MINNIE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V242000·2023-04-05

    Maserati Recalls 2023 MC20 Cielo for Windshield Frame Bonding Defect

    Maserati is recalling 2023 MC20 Cielo vehicles because insufficient windshield frame bonding could allow the frame to detach in a crash, increasing injury risk.

    Product
    MASERATI — MASERATI MC20 CIELO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V227000·2023-03-31

    Forest River Recalls 2023 East to West Travel Trailers Due to Drawbar Defect

    Forest River is recalling 2023 East to West Della Terra and Silver Lake travel trailers because the drawbar assembly may break, potentially allowing the trailer to detach.

    Product
    EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V228000·2023-03-30

    Honda Recalls 2007-2011 CR-V Vehicles for Frame Corrosion Risk

    Honda is recalling 2007-2011 CR-V vehicles sold or registered in specific states due to frame corrosion that could cause the rear trailing arm to detach.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V216000·2023-03-30

    Altec Recalls Digger Derricks and Aerial Devices Due to Missing Weld

    Altec is recalling 2016-2022 digger derricks and aerial devices because a missing weld on the rear pole rack could cause the pole to drop, increasing injury risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E022000·2023-03-20

    Meritor Recalls Front Drive Steer Axles Due to Loose Fasteners

    Meritor is recalling specific front drive steer axles because fasteners may not be tightened sufficiently. This defect could cause axle separation and loss of vehicle control.

    Product
    STEERING:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1205-2023·2023-03-08

    Sit to Stand STS500 Patient Lift Recalled Due to Loose Boom Fasteners

    Med-Mizer is recalling 37 units of the Sit to Stand STS500 Patient Lift due to risk of boom pivot failure caused by a loose securing nut and unsecured bolt on the boom flange.

    Product
    Sit to Stand STS500 Patient Lift
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·23E018000·2023-03-08

    AROW Recalls Emergency Exit Windows Due to Latch Failure Risk

    AROW Global Corp is recalling MV204 and MV207 emergency exit windows because the latch may fail during a crash, potentially allowing the window to open and increasing injury risk.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1204-2023·2023-03-08

    Med-Riser MR600 Patient Lift Boom Pivot Failure Risk Recall

    Med-Mizer, Inc. is recalling the Med-Riser MR600 Patient Lift due to risk that the boom pivot may fail if the securing nut loosens and the bolt becomes unsecured. Contact the manufacturer for instructions.

    Product
    Med-Riser MR600 Patient Lift
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·23V148000·2023-03-07

    Terex Advance Front Discharge Mixer Recall for Loose Axle Fasteners

    Terex Advance is recalling 2022 Front Discharge Mixer Commander vehicles because front-drive steer axle fasteners may not be tightened sufficiently, risking axle separation and loss of control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23C002000·2023-03-03

    Dorel Recalls Multiple Child Seat Models Due to Anchor Failure Risk

    Dorel Juvenile Group is recalling specific Safety 1st and Maxi-Cosi child seats because lower anchors may fail, allowing the seat to detach in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23137·2023-03-02

    TJX Office Chairs Recalled Due to Fall Hazard

    The TJX Companies is recalling approximately 81,700 office chairs because the back can break or detach from the seat base when occupied, posing a fall hazard. The firm has received 12 reports of the chair back failing, including 10 reports of injuries.

    Product
    Office Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V117000·2023-02-23

    Braun Recalls Demers Ambulances Due to Rear Step Welding Defect

    Braun Ambulances is recalling specific 2020 and 2022 Demers ambulances because the rear step may fail under weight due to incorrect welding, posing an injury risk.

    Product
    DEMERS — DEMERS MXP170Z, MXP150Z, MX164E, MX170E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23132·2023-02-23

    Zinus SmartBase Euro Slats Metal Platform Bed Frames Recalled for Collapse Hazard

    Zinus is recalling about 30,400 SmartBase Euro Slats metal platform bed frames because missing reinforcing brackets can cause the frame to collapse, creating an injury hazard. Consumers should stop using the bed frames and request a free repair kit.

    Product
    SmartBase® Euro Slats Metal Platform Bed Frames
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1107-2023·2023-02-15

    Surgical instrument tracker recalled for structural failure during use

    Trackx Technology is recalling 464 units of its Insight Base Modular Instrument Tracker because the device breaks and falls off from surgical instruments during procedures. No injuries have been reported.

    Product
    TrackX Insight Base Modular Instrument Tracker, 5L, REF #604-3TX, Sterile; and TrackX Insight Base Modular Instrument Tracker, 6.5L, Model #605-3TX, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide