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.

1401–1425 of 2056

  • SevereNHTSA·14V049000·2014-02-10

    EZ Loader Recalls 2013-2014 Boat Trailers Due to Wheel Cracking

    EZ Loader is recalling 2013-2014 boat trailers because specific trailer wheels may crack and separate, potentially causing a crash.

    Product
    EZ LOADER — EZ LOADER BOAT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0783-2014·2014-01-29

    Zimmer Segmental Systems Polyethylene Inserts Recalled for Loading Instructions

    Zimmer, Inc. is recalling Segmental Systems Polyethylene Inserts to update surgical instructions regarding excessive loading risks.

    Product
    Zimmer Segmental Systems; Polyethylene Inserts, Size B. Designed to address significant bone loss resulting from oncology, trauma, and/or salvage of previously failed arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14090·2014-01-24

    Ergotron Recalls Interactive Wall Mounts Due to Weld Failure Risk

    Ergotron is recalling interactive wall mounts because a weld can fail, causing the TV to fall. No injuries have been reported, but property damage occurred.

    Product
    Ergotron Interactive Wall Mounts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V011000·2014-01-23

    Corn Pro Deckover Flatbed Trailer Recall for Tail Pivot Box Failure

    Cornelius Manufacturing is recalling 2012-2014 Corn Pro Deckover Flatbed Trailers because welded boxes allowing the tail to pivot may fail, increasing accident risk.

    Product
    CORN PRO — CORN PRO DECKOVER FLATBED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0726-2014·2014-01-22

    Anspach Carbide Cutting Burrs Recalled Due to Fracture During Use

    The Anspach Effort, Inc. is recalling specific carbide cutting burrs because some fractured during use. The products are intended for cutting and shaping bone.

    Product
    Anspach Carbide Cutting Burrs: 2MM Carbide Fluted Ball, Standard, 8 Flutes - part #QD8-2SB-C-8F, 4MM Carbide Fluted Ball, 10 Flutes - part # QD8-4B-C-10F 5MM Carbide Fluted Ball, 10 Flutes - part #QD8-5B-C-10F 7MM Carbide Fluted Ball, 14 Flutes - part #QD8-7B-C-14F Anspach
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E002000·2014-01-17

    B&W Recalls Tow & Stow Adjustable Ball Mounts Due to Pin Fracture Risk

    B&W Custom Truck Beds is recalling specific Tow & Stow Adjustable Ball Mounts because the securing pins may fracture, potentially causing the trailer to separate from the vehicle.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0582-2014·2014-01-01

    Stryker Orthopaedics Recalls Rim Impactor Tips Due to Cracks and Fractures

    Stryker Howmedica Osteonics Corp. is recalling 1,690 Rim Impactor Tips used in MDM surgery due to complaints of cracks and fractures.

    Product
    Stryker Orthopaedics Rim Impactor Tip Product Usage: Used for MDM surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·14069·2013-12-19

    Playtex Recalls Hip Hammock Infant Carriers Due to Fall Hazard

    Playtex is recalling Hip Hammock infant carriers because buckles can crack or break, posing a fall hazard to children.

    Product
    Playtex Hip Hammock infant carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0484-2014·2013-12-18

    Trumpf Medical Systems Recalls Helion S and H300 Exam Lights

    Trumpf Medical Systems is recalling 287 Helion S and H300 exam lights because a plastic joint may fail due to fatigue after seven years of use.

    Product
    Helion S Exam Light or H300 The device is intended to locally illuminate an examination area of the patient's body with high intensity light in a clinic or doctor's practice.
    Category
    Medical Device
    Distribution
    16 states
  • HighNHTSA·13V623000·2013-12-16

    Hino Recalls 2013 NV8J Trucks for Incorrect Weight Documentation

    Hino is recalling 2013 NV8J trucks because vehicle documents show a higher weight rating than the actual modified rating, which could lead to overloading.

    Product
    HINO — HINO NV8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0417-2014·2013-12-04

    DePuy Orthopaedics Recalls HP M.B.T. Keel Punch Knee Instruments

    DePuy Orthopaedics is voluntarily recalling HP M.B.T. Keel Punch Knee Instruments because tabs on the connection end may fracture and remain in the patient.

    Product
    SIGMA¿ LCS¿ HIGH PERFORMANCE" MBT KEEL PUNCH NONCEMENTED Size 4-7 HP M.B.T. Keel Punch Knee Instrument is used to prepare the proximal tibial canal geometry to accept the final or definitive tibial tray used during total knee arthroplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0405-2014·2013-12-04

    Synthes Implant Holder Recalled Due to Breakage During Orthopedic Surgery

    Synthes USA HQ, Inc. is recalling 548 Synfix (TM)-LR Implant Holders because they may break at the interface between the implant and the holder.

    Product
    Synthes Implant Holder for Synfix (TM)-LR the Synthes Implant Holder for Synfix (TM)-LR is a non-powered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V608000·2013-12-04

    Triumph Recalls 2013 Trophy SE Motorcycles Due to Center Stand Defect

    Triumph is recalling 416 model year 2013 Trophy SE motorcycles because the left-hand center stand mount may fracture, potentially causing the bike to fall over while parked.

    Product
    TRIUMPH — TRIUMPH TROPHY SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14037·2013-12-04

    K2 Revo Kick Kickboards Recalled for Handle Detachment Hazard

    K2 Sports is recalling K2 Revo Kick kickboards/scooters because the front assembly can break, causing the handle to detach and posing a fall hazard to riders.

    Product
    K2 Revo Kick kickboards/scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0362-2014·2013-11-27

    Ossur Fixed Offset Adapter Recalled for Fatigue Cracks and Separation Risk

    Ossur North America Inc is voluntarily recalling 66 units of the A-642100 Fixed Offset Adapter because the component can develop fatigue cracks and separate completely during normal use.

    Product
    Fixed Offset Adapter, A-642100. The Offset Adapter is a fixed modular component which sets the tube 14.5 mm (0.57 inch) offset from the center line of the pyramid. It is made of a high-strength alloy with a pyramid receiver and is intended where there is a need to offset the t
    Category
    Medical Device
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0370-2014·2013-11-27

    FDA Recalls Medcare Max-500 Patient Lifts Due to Potential Load Failure

    Ergosafe Products LLC is recalling 97 Medcare Max-500 patient stands because the lift might fail with the labeled 500-lb load rating.

    Product
    Medcare Products Max-500 Stand, Total Support, patient stand, model #400006. The responsible firm name listed in the Operations Manual is Medcare Products, Burnsville, MN. Used for assisting patients/residents to a standing position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0342-2014·2013-11-27

    Trumpf TruSystem Surgical Table Leg Section Recall for Detachment Risk

    Trumpf Medical Systems is recalling 15 TruSystem Surgical Table Leg Section One Part Light components because the coupler point may detach from the frame.

    Product
    TruSystem Surgical Table (TS7000)  Leg Section One Part Light HU Use of the Leg Section One Part Light HU is permitted only with the TRUMPF TruSystem 7000 operating table. The operating table TruSystem 7000, in conjunction with operating table components is intended for the u
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0359-2014·2013-11-27

    Biomet Spine Recalls Polaris Translation Screws Due to Head Dissociation

    Biomet Spine is recalling 7,092 Polaris Translation Screws because the screw head may separate from the shaft. The recall covers nationwide distribution including Puerto Rico.

    Product
    BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for immobilization and stabilization as an adjunct to fusion as a pedicle screw fixation system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14033·2013-11-26

    Burley Recalls Tailwind Bicycle Racks for Trailercycles Due to Fall Hazard

    Burley Design is recalling Tailwind bicycle racks for trailercycles because the top portion can break, causing the trailercycle to disconnect and posing a fall hazard.

    Product
    Tailwind bicycle racks for trailercycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14027·2013-11-21

    ElliptiGO Recalls Outdoor Elliptical Cycles Due to Fall Hazard

    ElliptiGO is recalling about 7,200 outdoor elliptical cycles in the U.S. and Canada because the front fork or drive arm axles can detach, posing a fall hazard.

    Product
    ElliptiGO outdoor elliptical cycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V582000·2013-11-20

    Jet Co Aluminum Grain Trailers Recalled for Weak Top Rail

    Jet Co is recalling 2011-2012 aluminum grain trailers because a weak top rail may buckle, increasing crash risk.

    Product
    JET CO — JET CO ALUMINUM GRAIN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide