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.

1151–1175 of 2056

  • HighNHTSA·15V564000·2015-09-04

    Thomas Built Buses Recall Wheelchair Lifts Due to Bearing Defect

    Daimler Trucks North America is recalling 2006-2015 Thomas Built Buses equipped with certain Ricon wheelchair lifts. Defective pivot holes may allow bearings to move, risking platform failure and injury.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, SAF-T-LINER EF, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V565000·2015-09-04

    Thomas Built Buses Recall Wheelchair Lifts with Potential Bearing Failure

    Daimler Trucks North America is recalling 4,334 Thomas Built Buses equipped with specific Ricon wheelchair lifts due to a defect that could cause the platform to fall.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER FS65, SAF-T-LINER C2, SAF-T-LINER HDX, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V557000·2015-09-03

    Fontaine Recalls 2015 Traverse HT Trailers Due to Suspension Defect

    Fontaine Trailer Company is recalling 2015 Traverse HT trailers because a suspension member may separate from the trailer, increasing the risk of a crash.

    Product
    FONTAINE — FONTAINE TRAVERSE HT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15231·2015-09-03

    Cannondale Mountain Bicycles Recalled for Stem Failure and Fall Risk

    Cycling Sports Group is recalling about 23,000 Cannondale mountain bicycles because the OPI stem/steering tube can fail, posing a risk of injury from a fall.

    Product
    Cannondale mountain bicycles with OPI stem/steering tube
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2467-2015·2015-09-02

    Sunrise Medical Recalls Quickie IRIS Wheelchairs with Dynamic Backrest

    Sunrise Medical is recalling 64 Quickie IRIS wheelchairs because the backrest system may break, posing a risk of falls or injury to the occupant.

    Product
    Quickie IRIS Wheelchair. model EIZ4-2 in combination with option code 183M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2466-2015·2015-09-02

    Sunrise Medical Recalls Quickie and Zippie IRIS Wheelchairs with MONO Backrest

    Sunrise Medical is recalling 64 Quickie and Zippie IRIS wheelchairs because the MONO Backrest System may break, posing a risk of falls or injury to the occupant.

    Product
    Zippie IRIS Wheelchair. model EIZ5A in combination with option code 188M02 - MONO Backrest system with Dynamic Backrest option. Provide mobility to persons limited to a sitting position.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2367-2015·2015-08-26

    Teleflex Medical Recalls Sheridan Sher-I-BRONCH Endobronchial Tubes

    Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.

    Product
    HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Left sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring br
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2369-2015·2015-08-26

    Teleflex Sheridan SHER-I Bronch Accessory Pack Recalled for Connector Defect

    Teleflex Medical is recalling Sheridan SHER-I Bronch Accessory Packs because the double swivel connector may crack or separate on the endobronchial tube.

    Product
    HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a patient's upper airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15225·2015-08-26

    CAMP USA Recalls Blade Runner Crampons Due to Fall Hazard

    CAMP USA is recalling Cassin Blade Runner and Alpine crampons because the front part can break, posing a fall hazard. No injuries have been reported.

    Product
    Cassin Blade Runner and Blade Runner Alpine Crampons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V535000·2015-08-21

    Strick Van Trailer Recall for Suspension Pivot Bolt Failure Risk

    Strick is recalling 2014 Van Trailers with SAF-Holland suspension systems because pivot bolts may fail, potentially causing the axle to separate from the trailer.

    Product
    STRICK — STRICK VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E068000·2015-08-21

    Ricon wheelchair lifts recalled due to potential platform failure

    Ricon is recalling specific wheelchair lifts because oversized pivot holes may allow bearings to shift, potentially causing the platform to fall out of the vehicle.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2357-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Joint Breakage Risk

    Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia HD, User Manual #1513140. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2381-2015·2015-08-19

    Etac Relax Wall Mounted Shower Seat Recalled for Cracked Brackets

    Etac Supply Center Ab is recalling 13 units of the Etac Relax wall mounted shower seat due to reports of the wall bracket cracking or breaking.

    Product
    Etac Relax wall mounted shower seat The Etac Relax is a wall mounted shower seat designed as a seating and standing support for personal hygiene purposes for people with reduced mobility. The Etac Relax shower seat is used for sitting where space is restricted, and can be folded
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2356-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled Due to Joint Breakage Risk

    Trumpf Medical Systems is recalling ceiling-mounted surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruVidia SD, User Manual #1400191. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2353-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Spring Arm Defect

    Trumpf Medical Systems is recalling 9,287 surgical lighting systems because the front joint of the spring arm may break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,iLED 3/5, User Manual #1558932. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2354-2015·2015-08-19

    Trumpf Ceiling Mounted Surgical Lighting Systems Recalled for Spring Arm Defect

    Trumpf Medical Systems is recalling TruLight 3000/5000 surgical lights because the front joint of the spring arm could break at the monitor interface.

    Product
    Trumpf Ceiling Mounted Surgical Lighting Systems,TruLight 3000/5000, User Manual #1528403. The TRUMPF surgical lights are intended to locally illuminate an operating or examination area of the patient's body with a high intensity light.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15218·2015-08-18

    Rite Aid Recalls Outdoor Dining Sets Due to Fall Hazard

    Rite Aid is recalling about 13,000 outdoor dining sets because chair arms and legs can bend, causing users to fall and potentially be injured.

    Product
    Outdoor Dining Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2271-2015·2015-08-05

    Draeger Fabius MRI Anesthesia Machine Recalled for Magnetic Field Attraction

    Draeger Medical is recalling 373 Fabius MRI anesthesia machines because their parts can be loosened by the magnetic field of MRI equipment.

    Product
    Fabius MRI Anesthesia Machine; Fabius MRI is an inhalation anesthesia machine for use in MRI environments in operating, induction and recovery rooms.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2152-2015·2015-07-29

    Biomet Polaris 4.75 TI Spinal System Multiaxial Screws Recalled for Fatigue Strength

    Biomet Spine is recalling 4,765 units of Polaris 4.75 TI Spinal System multiaxial screws because they may not meet internal fatigue strength requirements.

    Product
    Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, Rx Only, REF 14-583020, Biomet Spine and Bone Healing Technologies. Spinal fixation component.
    Category
    Medical Device
    Distribution
    Distributed nationwide