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.

651–675 of 2094

  • HighFDA (Devices)·Z-0058-2021·2020-10-14

    Medline Recalls ClearPro Closed Suction Catheters Due to Assembly Separation

    Medline Industries is recalling 6,225 ClearPro Closed Suction Catheters because the catheter may separate from the device assembly during use.

    Product
    ClearPro Closed Suction Catheter, Model DYNCPDS14T, 14 Fr FOR ENDOTRACHEAL TUBE - Product Usage: Catheters are intended for endotracheal suction of adult patients with artificial airways. Single use only.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-3019-2020·2020-10-07

    Exactech Recalls Equinoxe Reverse Shoulder Compression Screw Kits

    Exactech is recalling Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kits because they may contain screws of incorrect length.

    Product
    Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
    Category
    Medical Device
    Distribution
    23 states
  • SevereNHTSA·20V614000·2020-10-06

    Ferrari Recalls 812 Superfast Vehicles for Rear Window Adhesion Defect

    Ferrari is recalling 2018-2020 812 Superfast vehicles because the rear window may have been bonded incorrectly, potentially leading to detachment and increased crash risk.

    Product
    FERRARI — FERRARI 812 SUPERFAST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V616000·2020-10-06

    REV Recalls 2019 Road Rescue Type I Ambulances for Door Latch Defect

    REV Ambulance Group is recalling 2019 Road Rescue Type I ambulances because incorrect material in door latches may prevent doors from opening, creating a lock-in risk.

    Product
    ROAD RESCUE — ROAD RESCUE TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V613000·2020-10-05

    Volvo Recalls 2020 VNL Trucks for Window Hinge Defect

    Volvo Trucks North America is recalling 2020 VNL vehicles because window hinges may fail if sleeper windows are open, posing a crash risk.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V605000·2020-10-02

    2021 Motorhome Bunk Bed Motor May Fail, Causing Bunk to Fall

    The P2K Bunk Bed System motor in certain 2021 Coachmen Sportscoach and Forest River Georgetown motorhomes may fail, causing the bunk to fall while the vehicle is in motion. This increases the risk of injury or a crash.

    Product
    COACHMEN — COACHMEN, FOREST RIVER SPORTSCOACH, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V608000·2020-10-02

    Mercedes-Benz Recalls 2019 C 300 for Center Console Lock Defect

    Mercedes-Benz is recalling 2019 C 300 vehicles because the center console lock may not function properly, increasing injury risk in rear-end crashes.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2941-2020·2020-09-30

    MicroPort Recalls PROFEMUR Titanium Hip Prosthesis Components Due to Fracture Reports

    MicroPort Orthopedics is recalling specific PROFEMUR Titanium hip prosthesis components due to reports of fractures after implantation.

    Product
    PROFEMUR Neck Long Titanium, Catalog Numbers: PHA01204, PHA01214, PHA01224, PHA01234, PHA01244, PHA01254, PHA01264. Hip prosthesis component.
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·20E065000·2020-09-09

    Horizon Global Recalls U-Haul, Draw-Tite, and Reese Towpower Trailer Hitches

    Horizon Global is recalling specific U-Haul, Draw-Tite, and Reese Towpower trailer hitches sold between November 2019 and August 2020 due to a defect that may prevent the pintle hook from locking securely.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2916-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes or tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 7.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensiti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2913-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 6.0 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensiti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2918-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect may cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 8.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensiti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2914-2020·2020-09-09

    Cardinal Health Recalls PROTEXIS Latex Micro Surgical Gloves Due to Defects

    Cardinal Health 200, LLC is recalling PROTEXIS Latex Micro Surgical Gloves because a degradation defect could cause holes and tears at the cuffs.

    Product
    PROTEXIS Latex Micro Surgical Gloves Size 6.5 - Product Usage: This surgeon s glove is a disposable device made of natural rubber latex or synthetic rubber intended to be worn by operating room personnel to be a barrier protection from contamination. Various thickness for sensiti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V521000·2020-08-28

    Heartland Bighorn Traveler landing legs may collapse causing trailer to drop

    Certain 2019-2021 Heartland Cyclone, 2020-2021 Bighorn Traveler, and 2020-2021 Elkridge recreational trailers may have insufficient bracing on the front landing legs, which could buckle and collapse while parked, causing the trailer to drop unexpectedly.

    Product
    HEARTLAND — HEARTLAND CYCLONE, ELKRIDGE, BIGHORN TRAVELER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V510000·2020-08-27

    Vac-Tron Recalls 140 Trucks for Rear Extremity Safety Defect

    Vac-Tron is recalling 140 trucks because the rear extends too far, increasing injury risk in rear-end crashes.

    Product
    VAC-TRON — VAC-TRON HTV 373 PTO, JTV 873 PTO, HTV 873 PTO, HTV 573 PTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2816-2020·2020-08-26

    DePuy Synthes LCP Plate Recall Due to Dimensional Tolerance Issues

    Synthes (USA) Products LLC is recalling 191 units of DePuy Synthes Trauma LCP One-Third Tubular Plates because dimensional features may be out of tolerance, potentially reducing locking strength.

    Product
    DePuy Synthes Trauma LCP One-Third Tubular Plate with Collar 8 Holes / 93mm - Product Usage: intended for fixation of fractures, osteotomies and non-unions of clavicle, scapula, olecranon, humerus, radius, ulna, pelvis, distal tibia and fibula, particularly in osteopenic bone. Pa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2817-2020·2020-08-26

    Golden Technologies Lift Chair Recalled for Suspected Poor Weld

    Golden Technologies is recalling 251 Model PR515 Lift Chairs due to a suspected poor weld on the back KD bar.

    Product
    Golden Technologies Model Number PR515 Lift Chair - Product Usage: is to provide lift assistance for persons who have difficulty rising from a seated position to a standing position.
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·20E057000·2020-08-20

    Motorcar Parts Recalls Duralast Brake Master Cylinders for Volkswagen Models

    Motorcar Parts of America is recalling specific Duralast brake master cylinders for Volkswagen vehicles due to a defect that may cause loss of braking.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V470000·2020-08-10

    Ford Recalls 2020 Lincoln Corsair for Rear Coil Spring Clearance Issue

    Ford is recalling 2,965 2020 Lincoln Corsair vehicles because rear coil springs may lack sufficient clearance, potentially breaking and affecting vehicle handling.

    Product
    LINCOLN — LINCOLN CORSAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V464000·2020-08-07

    Mercedes-Benz Recalls 2020 GLE 450 for Windshield Bonding Defect

    Mercedes-Benz is recalling one 2020 GLE 450 because the windshield may not be bonded correctly, which could reduce the effectiveness of the passenger air bag in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide