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.

1276–1300 of 2056

  • HighFDA (Devices)·Z-0228-2015·2014-11-26

    Monteris Medical Recalls FullFire Diffusing Tip Laser Probes Due to Tip Separation

    Monteris Medical is recalling 133 FullFire Diffusing Tip Laser Probes because the distal sapphire tip may separate from the probe.

    Product
    FullFire Diffusing Tip Laser Probe, REF: DTP101-01, DTP201-01, DTP301-01, DTP401-01, DTP501-01. These laser probes are part of the NeuroBlate System, a unique collection of MRI-compatible laser devices and accessories that create an MRI guided delivery of precision thermal ther
    Category
    Medical Device
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0202-2015·2014-11-19

    Medacta Recalls GMK Intramedullary Extension Rods Due to Breakage Reports

    Medacta is recalling GMK Intramedullary Extension Rods 100 mm after three reported cases of breakage during total knee replacement surgeries.

    Product
    GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to obtain correct leg alignment during total knee replacement.
    Category
    Medical Device
    Distribution
    1 state
  • HighNHTSA·14V742000·2014-11-19

    Champion Transit Buses Recalled for Wheelchair Lift Platform Cracking Risk

    Champion Bus is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.

    Product
    CHAMPION — CHAMPION HCAC, STACKED RAIL, PLATINUM SHUTTLE, DEFENDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0199-2015·2014-11-19

    DePuy ATTUNE Intuition Distal Femoral Jig Recall for Bushing Defect

    DePuy Orthopaedics is recalling ATTUNE Intuition Distal Femoral Jigs because a pin bushing defect could cause the plastic to fracture or displace during use.

    Product
    ATTUNE Intuition Distal Femoral Jig; sold non-sterile; product is wrapped in bubble wrap and then sealed inside a polyethylene bag
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2015·2014-11-19

    Roscoe Medical Recalls Transport Rollators Due to Caster Separation Risk

    Roscoe Medical Inc is recalling 831 Transport Rollators because the caster may separate from the frame, posing an injury risk to users.

    Product
    Transport Rollator with Padded Seat; Large 8-inch wheels with wheel locks (indoor and outdoor use), fold down footrests, ergonomic handles, curved padded backrest and handy wire basket for storage. Item# 30192 Burgundy each/Item# 30194 Blue each.. Transport Rollator is a whee
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15028·2014-11-18

    Black Diamond Recalls Whippet Ski Poles Due to Pick Breakage Risk

    Black Diamond Inc. is recalling Whippet and Carbon Whippet ski poles because the stainless steel pick can break, posing a risk of injury to users on slopes.

    Product
    Ski poles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14E078000·2014-11-17

    Carefree Latitude Awnings Recalled for Defective Screws on Motorhomes

    Carefree is recalling Latitude Awnings styles GX and G installed on motorhomes due to screws that may not meet specifications, posing a risk of the awning falling.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E074000·2014-11-14

    FLY Racing Recalls Certain Model .357 Motorcycle Helmets

    FLY Racing is recalling specific Model .357 helmets because the retention strap ring may separate in high heat, increasing crash injury risk.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V729000·2014-11-13

    Starcraft Bus Recalls Transit Buses Due to Wheelchair Lift Defect

    Forest River is recalling 2006-2012 Starcraft transit buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS STARQUEST, ULTRASTAR, ALLSTAR, XLT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E065000·2014-11-13

    Carefree Latitude Awning Recall Due to Cracking Mounting Brackets

    Carefree is recalling Latitude awnings because mounting brackets may crack, causing the awning to fall and potentially injure people underneath.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0172-2015·2014-11-12

    Stryker SmartLife Aseptic Housings Recalled for Welding Defect

    Stryker is recalling SmartLife Large Aseptic Housings because the top section may separate from the bottom due to insufficient welding.

    Product
    Stryker SmartLife Large Aseptic Housing REF 7126-120-000 Rx Only The SmartLife" Aseptic Housings are designed to be used in conjunction with the SmartLife Non-Sterile Batteries to provide power for System 7 Handpieces, Cordless Driver 4 Handpiece, and Sabo2 Sagittal Saw Hand
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V718000·2014-11-10

    Sutphen Aerial Devices Recalled for Potential Ladder Cable Failure

    Sutphen is recalling 2000-2014 aerial devices because a cable failure could cause the ladder to collapse, increasing injury risk.

    Product
    SUTPHEN — SUTPHEN SAI 110, SPI 112, SPH 100, SP 110
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V712000·2014-11-07

    Forest River Recalls 2015 Wildwood and Salem Trailers for Draw Bar Defect

    Forest River is recalling 2015 Wildwood and Salem Ice Cabin trailers because the draw bar may break, potentially causing the trailer to detach from the vehicle.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0142-2015·2014-11-05

    Mabis Recalls DMI Rollator Transport Chairs Due to Collapse Risk

    Briggs Medical Service Company is recalling 1,869 DMI Rollator Transport Chairs because they may collapse during use.

    Product
    DMI Duro-Med Industries Rollator Transport Chair; Wheel Size: 7 1/4"; Overall Width: 23 1/2"; Seat Height: 21 1/4"; Seat Size: 14" x 12 3/4"; Handle Height: 31" - 36"; Width Between Handles: 18"; Weight: 19 Lbs; Walking assistance device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V702000·2014-11-05

    Wabash National Van Trailer Recall for Cracking Pivot Bolts

    Wabash is recalling 2013 Van trailers because certain pivot bolts may crack, potentially causing the axle to separate and increasing crash risk.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V691000·2014-11-03

    Navistar Recalls IC Buses with Cracking Wheelchair Lifts

    Navistar is recalling certain IC buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    IC BUS — IC BUS CE, RE, FECB, FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V692000·2014-11-03

    Navistar Recalls IC School Buses with Cracking Wheelchair Lifts

    Navistar is recalling specific IC school buses because wheelchair lift platform side plates may crack. This defect could cause the platform to fall, increasing the risk of injury to the operator.

    Product
    IC BUS — IC BUS BE, AE, CE, RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0067-2015·2014-10-22

    Primus Medical Recalls AC Powered Adjustable Bed Frames

    Primus Medical LLC is recalling 1,726 AC powered adjustable bed frames used in nursing facilities because the head deck actuator bracket may separate from the frame.

    Product
    AC Powered adjustable bed frame. AC powered adjustable bed frame used in nursing facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide