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.

1551–1575 of 2056

  • HighNHTSA·12V535000·2012-11-06

    Fleetwood RV Recalls Motorhomes Due to Weak Entry Step Support

    Fleetwood RV is recalling certain 2010-2013 Storm, Terra, and Encounter motorhomes because the entry step lacks sufficient support and may collapse.

    Product
    FLEETWOOD — FLEETWOOD STORM, TERRA, ENCOUNTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0143-2013·2012-10-31

    SpiraLok 6.5mm Anchors Recalled Due to Post-Operative Fracture

    DePuy Mitek is recalling 372 units of SpiraLok 6.5mm anchors because they fractured after surgery, requiring patient revision.

    Product
    SpiraLok 6.5mm with Panacryl and needles Product Number: 222963 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0147-2013·2012-10-31

    DePuy Mitek Recalls SPIRALOK Bone Fixation Anchors Due to Fracture

    DePuy Mitek is recalling 66 SPIRALOK bone fixation anchors because they can fracture after surgery, requiring patients to undergo revision surgery.

    Product
    Screw, fixation, boneProduct Number: 222967 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0148-2013·2012-10-31

    DePuy Mitek Recalls Seven SpiraLok 5.0 Anchors Due to Fracture

    DePuy Mitek is recalling seven SpiraLok 5.0 anchors because they fractured after surgery, requiring patients to undergo revision procedures.

    Product
    SpiraLok 5.0 w/Needles with Orthocord Product Number: 222968 SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·13020·2012-10-25

    Tricam Recalls Easy Reach Step Stools Due to Fall Hazard

    Tricam Industries is recalling approximately 84,000 Easy Reach step stools sold at The Home Depot because the top step can break, posing a fall hazard.

    Product
    Step Stool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13018·2012-10-24

    Rivers Edge Recalls Hunter Tree Stands Due to Fall Hazard

    Rivers Edge is recalling about 14,000 hunter tree stands because snap-hook assemblies can fail, causing the stand and user to fall.

    Product
    Tree Stands for Hunters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0077-2013·2012-10-24

    Trumpf Medical Systems Recalls Helion and Xenion Surgical Lights

    Trumpf Medical Systems is recalling 275 Helion and Xenion surgical lights due to reported fractures of the front joint of the spring arm.

    Product
    Helion and Xenion surgical lights, 501/01 series KLM lights. The surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·13017·2012-10-23

    Dorel Recalls Eddie Bauer Rocking Wood Bassinets Due to Suffocation Hazard

    Dorel Juvenile Group is recalling approximately 97,000 Eddie Bauer Rocking Wood Bassinets because a locking mechanism failure can cause the bassinet to tip, posing a suffocation risk to infants.

    Product
    Eddie Bauer Rocking Wood Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0026-2013·2012-10-17

    OrthoHelix 3.2mm Cannulated Hex Driver Recall Due to Tip Breakage

    Orthohelix Surgical Designs Inc is recalling 47 non-sterile 3.2mm cannulated hex drivers because their tips are breaking while driving screws into patients.

    Product
    OrthoHelix Part #HCS-056-32 3.2MM Cannulated Hex Driver NON STERILE MAT: 465 SS The drivers are used to drive screws in the Mini MaxTorque Screw System, which is intended to be used to stabilize and aid in the fusion of fractures and osteotomies involving small bones of the h
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·12V515000·2012-10-17

    New Flyer Recalls 2010 Transit Buses Due to Weak Emergency Window Handles

    New Flyer is recalling 2010 GE35LFR and GE40LFR transit buses because emergency egress window handles may break before releasing the latch, potentially trapping passengers.

    Product
    NEW FLYER — NEW FLYER GE40LFR, GE35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13002·2012-10-02

    Haier Recalls 42-inch LED TVs Due to Stand Neck Breakage Risk

    Haier America is recalling 42-inch LED TVs because the stand's neck support can break, causing the TV to tip over. No injuries have been reported.

    Product
    Haier America Trading 42-inch LED Televisions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2383-2012·2012-09-26

    Varian Linear Accelerators Recalled Due to X-Jaw Carrier Alloy Defect

    Varian Medical Systems is recalling 221 linear accelerators worldwide because incorrect metal alloy in X-jaw carriers may cause cracking and undetected under-dosing.

    Product
    Varian brand Clinac, Trilogy, Novalis Tx, Unique, linear accelerators; Model Number: H14, H18, H29, Reference/FSCA Identifier: CP-08881; Product is manufactured and distributed by Varian Medical Systems Inc., Palo Alto, CA. 1) The Varian Low Energy Linear Accelerator is indic
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·12V462000·2012-09-20

    Nissan Recalls 2012 Frontier, Pathfinder, and Xterra for Front Wheel Hub Defect

    Nissan is recalling 2012 Frontier, Pathfinder, and Xterra vehicles because front wheel hubs may not meet hardness specifications, potentially leading to cracking and vehicle crashes.

    Product
    NISSAN — NISSAN FRONTIER, XTERRA, PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V463000·2012-09-20

    Vermeer Recalls HG6000TX Trailers Due to Kingpin Wear Risk

    Vermeer is recalling three HG6000TX horizontal grinder trailers because a defective kingpin may fail, causing the trailer to separate from the towing vehicle.

    Product
    VERMEER — VERMEER HG6000TX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12276·2012-09-13

    True Innovations Recalls Prestigio Office Chairs Due to Seat Plate Breakage

    True Innovations is recalling about 8,400 Prestigio office chairs because the seat plate can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a repair kit.

    Product
    Realspace Soho Prestigio High-Back Leather Chair
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2311-2012·2012-09-12

    Trumpf Acrobat 3000 Spring Arm Recalled for Welded Seam Cracks

    Trumpf Medical Systems is recalling Acrobat 3000 spring arms for iLED operating lights because cracks can form on the welded seam at the rear joint.

    Product
    Acrobat 3000 (AC3000) Spring Arm as support arm for iLED operating lights, TRUMPF Medizinsysteme GmbH + Co KG 82178 Puchheim. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patients body with a high intensity light.
    Category
    Medical Device
    Distribution
    7 states