The Recall Desk

Hazard

Structural Defect recalls

2,094 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,094
Critical
3
Severe
1,081
Most recent
2026-09-02

Of the 2,094 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 1,081 (52%) 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.

901–925 of 2094

  • SevereNHTSA·19V566000·2019-08-01

    Thor Motor Coach Recalls 2019-2020 Omni and Magnitude Motorhomes

    Thor Motor Coach is recalling 2019-2020 Omni and Magnitude motorhomes because the battery tray may detach, causing the vehicle to stall.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH MAGNITUDE, OMNI
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V563000·2019-07-31

    BMW Recalls 2018-2019 X3 and X4 Models for Seatback Welding Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V555000·2019-07-26

    Starcraft Bus Recalls 2018-2019 Models Due to Roof Hatch Handle Defect

    Forest River is recalling 2018-2019 Starcraft Allstar, Allstar XL, and Starlite vehicles because the roof hatch external handle may break, preventing emergency egress.

    Product
    STARCRAFT BUS — STARCRAFT BUS ALLSTAR, STARLITE, ALLSTAR XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V550000·2019-07-25

    Thomas Built Buses Recalling School Buses for Roof Hatch Handle Defect

    Daimler Trucks North America is recalling 2019-2020 Thomas Built school buses because the roof escape hatch handle may break, hindering emergency egress.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, MINOTOUR, SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1912-2019·2019-07-24

    Teleflex Neonatal Breathing Circuit Recall Due to Cracked Adaptors

    Teleflex is recalling 20 units of Neonatal ConchaSmart Breathing Circuits due to reported cracks on swivel wye adaptors observed prior to use.

    Product
    Teleflex HUDSON RDI NEONATAL ConchaSmart Breathing Circuit with Dual Heated Limb and ConchaSmart Column: a) REF 870-07KIT b) REF 870-09KIT Product Usage: The Neonatal ConchaSmart breathing circuits are intended to deliver humidified breathing gases for administration to a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V549000·2019-07-24

    Thomas Built Buses Recall Roof Escape Hatch Handle Defect

    Daimler Trucks North America is recalling specific Thomas Built Buses because the roof escape hatch handle may break, preventing emergency exit.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER HDX, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E047000·2019-07-19

    MORryde Recalls Fifth Wheel Pin Boxes Due to Short Bolts

    MORryde is recalling certain You Turn and Orbital Rotating Pin boxes because they may have shorter bolts than required, increasing the risk of a crash.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19E046000·2019-07-19

    MORryde Recalls Fifth Wheel Wedge Kits Due to Incorrect Bolts

    MORryde is recalling certain Orbital and You Turn Rubber Pin Box Wedge Kits because incorrect bolt lengths may prevent proper tightening, increasing crash risk.

    Product
    TRAILER HITCHES:FIFTH WHEEL ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1952-2019·2019-07-17

    Rinovum Recalls Revive Reusable Bladder Support Due to Structural Defect

    Rinovum Women's Health is recalling the Revive Reusable Bladder Support because the device may split or crack during its intended use life.

    Product
    Revive Reusable Bladder Support, Model No. 0025 - Product Usage: The Revive bladder support is intended for temporary management of urinary leakage caused by stress urinary incontinence (SUI) in women, 18 years and older. The device comes in a sealed box, and contains a reusable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1909-2019·2019-07-10

    Baxter Recalls Revaclear 400 Dialyzers Due to Potential Fiber Rupture

    Baxter Healthcare is recalling Revaclear 400 dialyzers because ruptured fibers may cause blood leaks during hemodialysis treatment.

    Product
    REVACLEAR 400 Dialyzer, Product Code 114746L Revaclear 300 and Revaclear 400 dialyzers are indicated for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V512000·2019-07-03

    Winnebago Forza Motorhomes Recalled for Storage Door Defect

    Winnebago is recalling 2017-2019 Forza motorhomes because the exterior storage compartment door may unexpectedly open while driving, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO FORZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1825-2019·2019-06-26

    FDA Recalls Covidien EGIA 30 Articulating Medical Devices

    The FDA is recalling 3,113,280 units of the EGIA 30 Articulating Medical device due to missing pin components that may cause incomplete staple formation and serious surgical complications.

    Product
    EGIA 30 ARTICULATING MED THICK SULU, Item Code EGIA30AMT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V493000·2019-06-26

    Subaru Recalls 2019 Legacy and Outback for Body Strength Defect

    Subaru is recalling 2019 Legacy and Outback vehicles because improperly applied spot welds may reduce body strength, increasing injury risk in a crash.

    Product
    SUBARU — SUBARU OUTBACK, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1828-2019·2019-06-26

    FDA Recalls Covidien EGIA 60 Articulating Extra Thick Sulu Devices

    The FDA is recalling 3,113,280 units of the EGIA 60 Articulating Extra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious surgical complications.

    Product
    EGIA 60 ARTICULATING EXTRA THICK SULU, Item code EGIA60AXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1827-2019·2019-06-26

    FDA Recalls 3.1 Million Covidien EGIA 45 Articulating Xtra Thick Sulu Devices

    The FDA is recalling 3,113,280 units of the EGIA 45 Articulating Xtra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious medical complications.

    Product
    EGIA 45 ARTICULATING XTRA THICK SULU, Item Code EGIA45AXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1758-2019·2019-06-26

    Cook Inc. Recalls Advance Enforcer 35 Focal Force PTA Balloon Catheters

    Cook Inc. is recalling 73 Advance Enforcer 35 Focal Force PTA Balloon Catheters because they may burst below the rated pressure, posing risks of vessel injury and balloon fragmentation.

    Product
    Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm, 5FR/135cm, Catalog Number ASB5-35-135-6-4, REF Number G35257 Product Usage: The Advance Enforcer 35 Focal-Force PTA Balloon Catheter is intended for percutaneous transluminal angioplasty (PTA) of lesions in perip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V450000·2019-06-13

    Roadtrek Motorhomes Recalled for Weak Second-Row Seat Anchor Brackets

    Erwin Hymer is recalling 2013-2019 Roadtrek motorhomes because second-row seat anchor brackets may lack sufficient strength, increasing injury risk in a crash.

    Product
    ROADTREK — ROADTREK CS ADVENTUROUS, RS ADVENTUROUS, E-TREK, TS ADVENTUROUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V445000·2019-06-12

    Porsche Recalls 2019-2020 Models for Driveshaft Bolt Tightening Issue

    Porsche is recalling 2019 911 GT2 RS and 2020 911 Carrera S Coupe vehicles because driveshaft bolts may not be properly tightened, increasing crash risk.

    Product
    PORSCHE — PORSCHE 911 CARRERA, 911 GT2
    Category
    Vehicle
    Distribution
    Distributed nationwide