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.

1376–1400 of 2056

  • SevereFDA (Devices)·Z-1542-2014·2014-05-14

    Med-Mizer RetractaBed Recall for Insufficient Welding on Foot Cross Tube

    Med-Mizer is recalling RetractaBed Clinical Contour adjustable beds due to insufficient welding on the foot cross tube, which may cause bed collapse or rollers to detach.

    Product
    RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 799, 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1541-2014·2014-05-14

    Med-Mizer Retractabed Recall for Insufficient Welding on Foot Cross Tube

    Med-Mizer is recalling 191 Retractabed Clinical Contour adjustable beds manufactured before June 7, 2008, due to insufficient welding that could cause bed collapse.

    Product
    RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed w/ 2 motors); 763 (3 motors); 763 A ( 3 motors, autocontour) 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14168·2014-05-05

    Cannondale Recalls 2014 Tandem Bicycles Due to Fork Breakage Risk

    Cycling Sports Group is recalling about 80 2014 Cannondale tandem bicycles because the fork can break, causing riders to lose control and potentially be injured.

    Product
    2014 Cannondale Tandem Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14159·2014-04-24

    Felt Triathlon Bicycles Recalled Due to Fork Steer Tube Breakage Risk

    Felt Bicycles is recalling 2008 and 2010 triathlon models because the steer tube can break, causing loss of control and injury.

    Product
    2008 Felt S22 and S32 Triathlon Bicycles and 2010 Felt S32, B12, B14 and B16 Triathlon Bicycles.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2014·2014-04-16

    Medcare Floor Lifts Recalled Due to Potential Pin Failure

    ErgoSafe Product LLC is recalling Medcare Floor Lifts manufactured between 2010 and 2012 because a design pin may break over time.

    Product
    400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage: The intended use is a patient hanger bar (400600) attached to a 400003 or 400013 floor lift used to lift, transfer or position clients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V189000·2014-04-10

    MV Agusta Recalls 2014 Motorcycles Due to Swingarm Bolt Failure Risk

    MV Agusta is recalling 223 model year 2014 motorcycles because a swingarm bolt may fail, increasing the risk of a crash.

    Product
    MV AGUSTA — MV AGUSTA F3 800, BRUTALE RR, F3 675, RIVALE 800
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1272-2014·2014-04-02

    Siemens AXIOM Artis Systems Recalled for Potential Gantry Drop Risk

    Siemens is recalling 37 AXIOM Artis angiography systems because a cooling unit defect may cause a system failure and gantry drop.

    Product
    AXIOM Artis Systems Product usage: Artis zee is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V141000·2014-03-25

    KZRV Recalls 2014 Sportsmen Trailers Due to Axle Defect

    KZRV is recalling 2014 Sportsmen 290IKSS travel trailers because the axles may not support the trailer's weight, increasing crash risk.

    Product
    SPORTSMEN — SPORTSMEN 290IKSS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V122000·2014-03-13

    Terex Recalls 2014 TZ-50 Aerial Work Platforms Due to Weld Defects

    Terex is recalling 2014 TZ-50 trailer-mounted aerial work platforms because a welding process change may cause cracks in the boom section, risking platform failure.

    Product
    TEREX — TEREX TZ-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1150-2014·2014-03-12

    Shimadzu Recalls Mobile X-ray Systems Due to Metal Plate Cracking Risk

    Shimadzu Medical Systems is recalling 56 mobile X-ray systems because a connecting metal plate may crack, posing a structural safety risk.

    Product
    Mobile X-ray System, Model: MUX-100, MUX-100H Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannnot move and/or of outpatients in emergency
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1127-2014·2014-03-12

    Carestream Recalls Kodak 2100 Intraoral X-Ray Systems Due to Arm Breakage

    Carestream Health is recalling Kodak 2100 Intraoral X-Ray Systems because the device arms may break early. The recall covers 347 units distributed in the US and Canada.

    Product
    Model Kodak 2100 Intraoral X-Ray System, Catalog Numbers 5303144, 8011579 -- Carestream Health, Inc. 150 Verona Street Rochester, NY 14608 -- Made in France -- TROPHY 77435 Marne La Vallee --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray, Extraora
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1086-2014·2014-03-05

    Stryker Recalls Static Inserter Assemblies Due to Weld Fracture Complaints

    Stryker Spine is recalling 21 units of Specialty Straight Static Inserter Assemblies because customers reported fractures along the weld binding the handle to the shaft.

    Product
    Specialty Straight Static Inserter Assembly Product Usage: This instrument is a part of the Navigator product brand . It is used for implant insertion in to the disc space. The AVS navigator Peek Spacer System offers implants that are interbody fusion devices intended for
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V097000·2014-03-04

    Ford E-Series CNG Conversion Recall for Rear Cylinder Bracket Failure

    Landi Renzo USA is recalling 2011-2014 Ford E-150, E-250, and E-350 vans modified for CNG because rear cylinder brackets may fail, risking a gas leak and fire.

    Product
    FORD — FORD E-350, E-250, E-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1000-2014·2014-02-26

    Medtronic Recalls Select 3D and CAP Arterial Cannulae Due to Splitting

    Medtronic is recalling Select 3D and Select CAP Arterial Cannulae because the cannula body may split near the suture collar.

    Product
    Medtronic Intersept Custom Tubing Pack which contain Select 3D or Select CAP Arterial Cannulae. Model 3Y90R3, the following model is only approved in Europe C300901B. Sterilized using Ethylene Oxide. Non-pyrogenic. The design and components of this product are specified b
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0995-2014·2014-02-26

    Medtronic Recalls Select 3D Arterial Cannulae Due to Body Splitting

    Medtronic is recalling Select 3D Arterial Cannulae because the device body may split near the suture collar.

    Product
    Medtronic Select 3D Arterial Cannulae. Vented, models 78618 (18 Fr.) and 78620 (20 Fr.). Non-Vented Cannulae, models 78718 (18 Fr.) and 78720 (20 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Select 3D Arterial Cannulae both have clear flexible, thin wall wi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0996-2014·2014-02-26

    Medtronic Recalls Select 3D Arterial Cannulae Due to Body Splitting

    Medtronic is recalling Select 3D and Select CAP Arterial Cannulae because the cannula body may split near the suture collar.

    Product
    Medtronic Select 3D Arterial Cannulae. Vented, model 78622 (22 Fr.). Non-Vented Cannulae, model 78722 (22 Fr.). Sterilized using Ethylene Oxide. Non-pyrogenic. The Cannula consists of a curved, angled or beveled tip with or without flange that is permanently attached to
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14113·2014-02-25

    Rollerblade USA Recalls Tempest Inline Skates Due to Fall Hazard

    Rollerblade USA is recalling about 11,800 pairs of Tempest inline skates because misaligned mounting holes can cause the boot to separate from the frame, posing a fall hazard.

    Product
    Rollerblade® Tempest Inline Skates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0964-2014·2014-02-19

    Stryker Accolade Broach Handle Recalled Due to Impaction Plate Fracture

    Stryker Howmedica Osteonics Corp. is recalling 211 units of the Navigation Compatible Accolade Broach Handle because the impaction plate may dissociate or fracture from the main body.

    Product
    Stryker Orthopaedics Navigation Compatible Accolade Broach Handle 1 single unit to a package Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 Meyzieu Cedex France Made in USA non-sterile
    Category
    Medical Device
    Distribution
    5 states
  • SevereNHTSA·14V055000·2014-02-11

    Freedom Motors Recalls Wheelchair-Accessible Vans Due to Rear Axle Cracks

    Freedom Motors is recalling certain 2008-2010 Dodge, Chrysler, and 2009 Volkswagen wheelchair-accessible vans because the rear axle may crack and fail, increasing crash risk.

    Product
    DODGE — DODGE, VOLKSWAGEN, CHRYSLER GRAND CARAVAN, ROUTAN, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide