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.

726–750 of 2056

  • SevereFDA (Devices)·Z-2594-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Infinity XR2 Base Units Due to Fracture Risk

    Integra LifeSciences is recalling Mayfield Infinity XR2 Low Profile Base Units because the knob assembly in the swivel adapter may fracture or break during use.

    Product
    MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2595-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Spine Table Adaptors Due to Fracture Risk

    Integra LifeSciences is recalling 95 Mayfield Spine Table Adaptors because the knob assembly may fracture during use, posing a risk to patients.

    Product
    MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT, Part Number A2600R The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2593-2018·2018-08-08

    MAYFIELD Infinity XR2 Base Unit Recalled Due to Fracture Risk

    Integra LifeSciences is recalling 17 MAYFIELD Infinity XR2 Base Units because the knob assembly may fracture during use.

    Product
    MAYFIELD Infinity XR2 Base Unit-Extended, Part Number A2079E The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2571-2018·2018-08-08

    Cayenne Medical Recalls Quattro Link Drills Due to Breakage Trend

    Cayenne Medical Inc. is recalling 229 Quattro Link drills because a review of complaints identified a trend for the devices breaking.

    Product
    Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300; b. Quattro Drill 2.4mm, Hard Bone, Model Number CM-9324
    Category
    Medical Device
    Distribution
    36 states
  • SevereNHTSA·18V520000·2018-08-07

    Terex Recalls 2015-2018 Digger Derricks Due to Weld Defect

    Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.

    Product
    TEREX — TEREX GENERAL 80, C4000, C6000, C5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E078000·2018-08-03

    Honda Recalls Africa Twin Centerstand Kits Due to Detachment Risk

    Honda is recalling Genuine Accessory Centerstand Kits for 2016-2018 Africa Twin motorcycles because a broken circlip can cause the stand to detach, creating a road hazard or causing the bike to fall.

    Product
    HONDA — HONDA CRF1000A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E064000·2018-07-30

    TAP Recalls Pro Comp Steering Knuckles for Nissan Titan Vehicles

    TAP Worldwide LLC is recalling Pro Comp aftermarket steering knuckles for Nissan Titan vehicles because they may deform or fracture under high loads, potentially causing loss of control.

    Product
    STEERING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V499000·2018-07-30

    Keystone Recalls 2019 Summerland Trailers Due to Propane Bracket Defect

    Keystone is recalling 2019 Summerland recreational trailers because the propane bottle brackets may break, allowing the cylinder to detach and increasing the risk of injury or crash.

    Product
    KEYSTONE — KEYSTONE SUMMERLAND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E070000·2018-07-30

    TAP Recalls G2 Axle Housings Due to Potential Weld Failure

    TAP Worldwide is recalling G2 Axle and Gear aftermarket axle housings because weak welds may allow the axle tube to rotate, increasing crash risk.

    Product
    POWER TRAIN:AXLE ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V495000·2018-07-27

    Trail King Recalls 2016-2018 Dolly Trailers Due to Frame Crack Risk

    Trail King is recalling 2016-2018 Dolly trailers because the frame channel may crack, potentially causing the frame rail to separate and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING DOLLY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E061000·2018-07-25

    Rock Run Recalls LP Bottle Ring Brackets for Propane Tank Safety

    Rock Run Industries is recalling LP Bottle Ring Brackets that may break, potentially causing propane cylinders to fall from vehicles.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18190·2018-07-24

    Ross Stores Recalls Bistro Chairs Due to Frame Breakage and Fall Hazard

    Ross Stores is recalling Bronze Hammered bistro chairs because the frames can break, posing a fall hazard. Consumers should stop using the chairs and return them for a full refund.

    Product
    Bistro chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2397-2018·2018-07-18

    Stryker Recalls Specific Femoral Nail Due to Potential Breakage Risk

    Stryker GmbH is recalling specific femoral nails due to potential manufacturing defects that could cause the device to break prematurely.

    Product
    Femoral Nail, A/R T2 Femur ¿15x240 mm, Product Number 18251524S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2394-2018·2018-07-18

    Stryker Recalls Two Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling two femoral nails that may have non-conforming cannulation, potentially leading to reduced strength and premature breakage.

    Product
    Femoral Nail, A/R T2 Femur ¿10x320 mm, Product Number 18251032S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2403-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, LEFT T2 GTN ¿12x360 mm, Product Number 18501236S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2407-2018·2018-07-18

    Stryker Recalls Ankle Arthrodesis Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling specific ankle arthrodesis nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Ankle Arthrodesis Nail, right T2 Ankle ¿10x300mm, Product Number 18191030S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2398-2018·2018-07-18

    Stryker Recalls Seven Femoral Nails Due to Potential Breakage Risk

    Stryker GmbH is recalling seven femoral nails because non-conforming cannulation may reduce strength and cause premature breakage.

    Product
    Femoral Nail, A/R, R1500 T2 Femur ¿10x320 mm, Product Number 18281032S
    Category
    Medical Device
    Distribution
    8 states
  • SevereFDA (Devices)·Z-2405-2018·2018-07-18

    Stryker Recalls Femoral Nails Due to Potential Premature Breakage

    Stryker GmbH is recalling specific femoral nails because non-conforming cannulation may reduce component strength and lead to premature breakage.

    Product
    Femoral Nail, RIGHT T2 GTN ¿9x320 mm, Product Number 18510932S
    Category
    Medical Device
    Distribution
    8 states