The Recall Desk

Hazard

Structural Failure recalls

2,074 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,074
Critical
11
Severe
1,064
Most recent
2026-10-29

Of the 2,074 structural failure recalls we have scored against our rubric, 11 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,064 (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.

251–275 of 2074

  • HighFDA (Devices)·Z-0670-2024·2024-01-17

    Townsend Design Custom SPRYSTEP Ankle-Foot Orthosis Recalled for Structural Failure Risk

    Townsend Design is recalling 248 units of CUSTOM SPRYSTEP ankle-foot orthotics for potential air pockets that could cause complete structural failure and loss of ankle support.

    Product
    CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040
    Category
    Medical Device
    Distribution
    48 states
  • HighFDA (Devices)·Z-0671-2024·2024-01-17

    SPRYSTEP VECTOR Ankle-Foot Orthosis Recalled for Structural Failure Risk

    Townsend Design is recalling the SPRYSTEP VECTOR custom ankle-foot orthosis due to potential air pockets between material layers that could cause complete structural failure. Users should stop using the device and contact the manufacturer.

    Product
    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037
    Category
    Medical Device
    Distribution
    48 states
  • HighCPSC·24078·2024-01-11

    Millions of New Age Furniture Tip Restraint Kits Recalled for Tip-Over and Entrapment Hazard

    Plastic New Age furniture tip restraint kits can break or become brittle, allowing anchored clothing storage units to detach and tip over, creating a hazard to children. Consumers should check manufacture dates and contact Alliance4Safety for free replacements.

    Product
    New Age Industries ("New Age") Furniture tip kits or tip restraints
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V003000·2024-01-05

    Forest River Recalls 2020 Cherokee Travel Trailers Due to Draw Bar Defect

    Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V002000·2024-01-04

    Terex Advance Concrete Mixer Trucks Recalled for Drum Separation Risk

    Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.

    Product
    TEREX ADVANCE — TEREX ADVANCE COMMANDER, CHARGER, MM300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E001000·2024-01-03

    Spektrum Brakes Recalls Dynamic Friction R1 Brake Rotors Due to Fracture Risk

    Spektrum Brakes is recalling Dynamic Friction R1 brake rotors because the hub can fracture, causing a loss of braking ability and increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:ROTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V892000·2023-12-22

    Alamo Recalls Old Dominion Brush Units Due to Hoist Bolt Failure Risk

    Alamo Group is recalling 2021-2023 Old Dominion Brush Company units because a hoist bolt can shear, causing the dump body to drop and potentially injure people.

    Product
    OLD DOMINION BRUSH CO. — OLD DOMINION BRUSH CO. TRUCK MOUNTED UNIT, TRAILER MOUNT UNIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V875000·2023-12-21

    Daimler Recalls 2019-2021 Sprinter Vans for Frame Fastener Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans because missing frame fasteners may reduce stability and structural integrity.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 3500, SPRINTER 2500, SPRINTER 1500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·24068·2023-12-21

    TJX Foldable Wood and Rope Bistro Set Chairs Recall Due to Fall Hazard

    TJX is recalling about 29,000 foldable wood and rope bistro set chairs because the wooden frame can break or collapse when occupied, creating a fall hazard. The company has received eight reports of frame breakage, including six reports of minor injuries such as bruising and ankle strain.

    Product
    Foldable wood and rope bistro set chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0505-2024·2023-12-20

    Philips Panorama MR System Structural Failure Risk from Helium Gas Pressure

    Philips Panorama 1.0T MR Systems (Models 781250, 781350) may experience structural failure during helium quench events, releasing pressurized gas and debris that could cause helium exposure, asphyxia, and injury to patients and operators.

    Product
    Panorama 1.0T HFO, Magnetic Resonance (MR) System; Model Numbers 781250 and 781350. Philips Magnetic Resonance (MR) systems are Medical Electrical Systems for use as a diagnostic device.
    Category
    Medical Device
    Distribution
    34 states
  • SevereNHTSA·23V851000·2023-12-15

    Mercedes-Benz Recalls 2022-2023 AMG G63 Due to Rear Axle Cracks

    Mercedes-Benz is recalling 2022-2023 AMG G63 vehicles because the rear axle differential housing may crack, potentially causing oil leaks or axle failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24734·2023-12-14

    Collegiate English Horse-Riding Saddles Recalled for Fall Injury Risk

    WeatherBeeta USA is recalling about 2,300 Collegiate English horse-riding saddles because the rivet or stirrup bar can break, causing the rider to fall. One fall injury has been reported.

    Product
    Collegiate English Horse-Riding Saddles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2024·2023-12-13

    NovoTHOR Gen 2.0 Light Therapy Bed Canopy Detachment Due to Ball Stud Failure

    Thor Photomedicine is recalling 19 NovoTHOR Gen 2.0 red light therapy beds due to ball stud component failures that can cause canopy detachment or difficulty in lifting. The beds were distributed worldwide.

    Product
    NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2024·2023-12-13

    Red Light Therapy Bed Canopy Strut Detachment Risk Nationwide

    Thor Photomedicine is recalling six THOR NOVO GEN 2.0 XL whole body red light therapy beds due to ball stud component failure. The defect causes gas strut detachment, making the canopy difficult to lift.

    Product
    G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V820000·2023-12-06

    Ducati Recalls XDiavel Motorcycles Due to Passenger Backrest Defect

    Ducati is recalling 2016-2023 XDiavel S and STD motorcycles because the passenger backrest may break, increasing the risk of the passenger falling off.

    Product
    DUCATI — DUCATI XDIAVEL S, XDIAVEL STD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24026·2023-11-16

    Tractor Supply Red Shed Hammock Swing Chairs Recalled Due to Fall Hazard

    Tractor Supply is recalling about 7,500 Red Shed® Hammock Swing Chairs because the plastic buckle supporting the back can break while someone is seated, causing a fall. The company has received 13 reports of buckle or stitching failures, including three falls.

    Product
    Red Shed® Hammock Swing Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0275-2024·2023-11-15

    Philips DigitalDiagnost C90 Radiographic Systems Recalled for Ceiling Mount Failure

    Philips is recalling 33 DigitalDiagnost C90 radiographic imaging systems nationwide due to potential structural failure of ceiling-mounted units. Equipment may fall, creating injury risk.

    Product
    DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0274-2024·2023-11-15

    DigitalDiagnost 4 Radiographic Systems Risk of Ceiling Mount Failure

    DigitalDiagnost 4 High Performance radiographic systems may fail and fall from ceiling mounts. The FDA recalls 366 units distributed nationwide.

    Product
    DigitalDiagnost 4 High Performance, used to acquire, process, store, display and export digital radiographic images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0156-2024·2023-11-01

    Omega Medical Imaging Monitor Suspension Actuator Separation Risk

    Omega Medical Imaging is recalling 52 monitor suspension systems (Part Number 1000-0085) manufactured 2012–2019 in which the actuator may separate from the pivot mechanism. An installed safety cable contained one such failure, but the structural issue poses a falling hazard. No injuries reported.

    Product
    Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V681000·2023-10-12

    GMC Acadia and Cadillac Windshield Detachment Risk Recall

    General Motors is recalling 2023 GMC Acadia vehicles and certain 2024 Cadillac models due to windshields that may not be properly bonded to the vehicle body. A detached windshield during a crash could increase the risk of injury.

    Product
    GMC — GMC, CADILLAC ACADIA, XT6, XT5
    Category
    Vehicle
    Distribution
    Distributed nationwide