The Recall Desk

Hazard

Structural Defect recalls

2,114 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,114
Critical
3
Severe
1,157
Most recent
2026-10-22

Of the 2,114 structural defect recalls we have scored against our rubric, 3 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,157 (55%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all structural defect 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.

1026–1050 of 2114

  • SevereFDA (Devices)·Z-0288-2019·2018-11-07

    Stryker Recalls Hoffmann LRF Hexapod Struts Due to Pin Fit Defect

    Stryker GmbH is recalling 578 Hoffmann LRF Hexapod Struts because a manufacturing defect may cause the pin to displace, compromising the stability of the orthopedic frame.

    Product
    Hoffman LRF Hexapod Strut, Extra Short 89mm-109mm, Model Number 4935-0-010. Product Usage - The Hoffmann LRF System is indicated in pediatric patients and adults for the treatment and fixation of: Open and closed fractures Post-traumatic joint contracture which has resulted…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V781000·2018-11-06

    Lotus Recalls 2018 Evora Vehicles for Steering Column Assembly Error

    Lotus is recalling 2018 Evora vehicles because an assembly error may prevent the steering column from collapsing properly in a frontal collision, increasing injury risk.

    Product
    LOTUS — LOTUS EVORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0198-2019·2018-10-31

    Bovie J-Plasma Precise 360 Handpiece Recalled for Tip Separation Risk

    Bovie Medical Corporation is recalling J-Plasma Precise 360 handpieces because the PEEK tip may separate and remain in patient tissue.

    Product
    J-Plasma Precise 360, single use, disposable. The Bovie J-Plasma Precise 360 Handpiece is used for the delivery of helium gas plasma for cutting, coagulation, and ablation of soft tissue during open and laparascopic surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V758000·2018-10-26

    Isuzu and Chevrolet Trucks Recalled for Cab Tilt-Lock Warning Defect

    Isuzu is recalling 2018-2019 Chevrolet Low Cab Forward 6500 and Isuzu FTR trucks because the cab tilt-lock may not provide an adequate warning after servicing.

    Product
    ISUZU — ISUZU, CHEVROLET FTR, LOW CAB FORWARD 6500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V755000·2018-10-25

    BMW Recalls Diesel Vehicles Due to EGR Cooler Leak Fire Risk

    BMW is recalling specific 2013-2018 diesel models because a leaking EGR cooler can cause the intake manifold to melt, increasing the risk of a fire.

    Product
    BMW — BMW 328D, X5, 535D, X3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0120-2019·2018-10-24

    A M Systems Recalls Disposable Smooth Interior Tubing for Pulmonary Equipment

    A M Systems Inc is recalling 610 units of Disposable Smooth Interior Tubing because the tubing may pull apart when stretched.

    Product
    Disposable Smooth Interior Tubing Material: Polyethylene EVA copolymer. This tubing is supplied non-sterile P/N: 1024920 Rev. 01 Low temperature smooth interior tubing is a disposable pulmonary equipment interconnect used in ventilation and aesthesia machines.
    Category
    Medical Device
    Distribution
    3 states
  • HighNHTSA·18V722000·2018-10-15

    Forest River Recalls School Buses Due to Seat Foam Impact Defect

    Forest River is recalling certain Starcraft and StarTrans school buses because the seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, STARTRANS QUEST, PRODIGY, SENATOR II, QUEST XL
    Category
    Vehicle
    Distribution
    Distributed nationwide