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.

226–250 of 2094

  • HighNHTSA·24V489000·2024-06-28

    Coachmen Cross Trail Motorhomes Recalled for Ladder Receiver Defect

    Forest River is recalling 2024-2025 Coachmen Cross Trail motorhomes because the ladder receiver may be installed without a backer, causing the ladder to detach.

    Product
    COACHMEN — COACHMEN CROSS TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V485000·2024-06-27

    Micro Bird Transit Bus Recall for Rear Emergency Door Handle Defect

    Micro Bird is recalling 794 transit buses because the rear emergency door handle may break, potentially delaying emergency access.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS, G5 TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V484000·2024-06-27

    Micro Bird Recalls School Buses Due to Rear Emergency Door Handle Defect

    Micro Bird is recalling 22,582 school buses because the rear emergency door handle may break, potentially delaying emergency access.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS, G5 SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V462000·2024-06-20

    International truck tie rod ball studs were incorrectly heat treated

    Navistar is recalling certain 2025 International HV, LT, MV and RH trucks because tie rod ball studs may have been incorrectly heat-treated and can break. 116 units affected.

    Product
    INTERNATIONAL — INTERNATIONAL RH, HV, MV, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V465000·2024-06-20

    Audi e-tron GT front axle brake hoses may tear and leak

    Volkswagen is recalling certain 2022-2024 Audi RS e-tron GT and e-tron GT vehicles because the front axle brake hoses can develop tears, causing a leak and brake circuit failure.

    Product
    AUDI — AUDI E-TRON GT, RS E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V454000·2024-06-18

    Entrans Recalls 2017 Polar Tank ARJH Trailers Due to Weld Defect

    Entrans is recalling 2017 Polar Tank ARJH trailers because improper tank welding may cause leaks, creating a road hazard and increasing crash risk.

    Product
    POLAR TANK — POLAR TANK ARJH TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V429000·2024-06-12

    Forest River Recalls School Buses Due to Insufficient Crash Protection

    Forest River is recalling 3,192 school buses because the restraining barrier may not provide sufficient protection in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, FOREST RIVER BUS PRODIGY, QUEST, QUEST XL, STARCRAFT ALLSTAR MPV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V431000·2024-06-12

    Endera Recalls 2021-2024 School Buses Due to Missing Seat Washers

    Endera is recalling 2021-2024 school buses because seat assemblies may lack reinforcing washers, causing non-compliance with safety standards and increasing injury risk.

    Product
    ENDERA — ENDERA SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V433000·2024-06-12

    2025 Kenworth and Peterbilt Trucks Steering Linkage Defect

    PACCAR is recalling 2025 Kenworth and Peterbilt trucks due to improperly heat-treated ball studs in steering assemblies that may break, causing loss of steering control.

    Product
    KENWORTH — KENWORTH, PETERBILT T880, T480, T380, T280
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1981-2024·2024-06-12

    Vascular graft recalled for reported swivel rod separation from core

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of the swivel rod separating from the swivel core. Patients and healthcare providers should contact the manufacturer for guidance.

    Product
    ADVANTA VXT, 8X80, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2008-2024·2024-06-12

    FLIXENE vascular graft recalled for slider separation defect

    Atrium Medical recalls FLIXENE vascular grafts due to reported separation between the slider rod and swivel core. Affected grafts may fail to function properly if deployed.

    Product
    FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1978-2024·2024-06-12

    ADVANTA VXT Vascular Graft Recalled for Component Separation

    ADVANTA VXT vascular grafts are recalled due to reported separation of the Slider GDS Swivel Rod from the Swivel Core, creating a gap between components.

    Product
    ADVANTA VXT, 7X70, 1GDS, NH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2007-2024·2024-06-12

    FLIXENE Vascular Graft Recall for Swivel Rod Component Separation

    Atrium Medical is recalling FLIXENE vascular grafts due to complaints of separation between the Swivel Rod and Swivel Core components. The recall affects 53,308 units worldwide, including 11,236 in the US.

    Product
    FLIXENE, 6X30, 1GDS, GW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1954-2024·2024-06-12

    ADVANTA VXT vascular graft recalled for slider rod separation

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to complaints of separation between the slider rod and swivel core, which could affect proper device function.

    Product
    ADVANTA VXT, 5X50, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2009-2024·2024-06-12

    Vascular graft recalled for swivel rod separation risk

    FDA recalls Atrium Medical's FLIXENE vascular grafts due to reports of the swivel rod separating from the core, potentially compromising device integrity.

    Product
    FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1987-2024·2024-06-12

    Advanta VXT vascular grafts recalled for swivel rod separation

    Atrium Medical Corporation is recalling the Advanta VXT vascular graft due to reports of the swivel rod separating from the swivel core. The recall affects approximately 53,308 units distributed in the United States and worldwide.

    Product
    ADVANTA VXT, 7X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1989-2024·2024-06-12

    ADVANTA VXT Vascular Graft Recalled for Swivel Rod Separation Risk

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts after reports of separation between the Slider GDS Swivel Rod and Swivel Core. This structural defect could affect device performance.

    Product
    ADVANTA VXT, 6X80, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1960-2024·2024-06-12

    Vascular graft devices recalled due to slider component separation

    Atrium Medical is recalling ADVANTA VXT vascular grafts following complaints of separation between the slider component and swivel core.

    Product
    ADVANTA VXT, 7X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2024·2024-06-12

    Vascular graft component separation reported in Advanta VXT devices

    Atrium Medical Corporation recalls Advanta VXT vascular grafts due to separation of internal swivel components. Approximately 53,308 units worldwide are affected, with the slider GDS swivel rod potentially separating from its core.

    Product
    ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1958-2024·2024-06-12

    Vascular graft slider component separation poses implant failure risk

    Atrium Medical is recalling ADVANTA VXT vascular grafts due to separation of the slider swivel rod from its core. This structural defect could lead to device failure. Over 53,000 units are affected worldwide.

    Product
    ADVANTA VXT, 5X70, 1GDS, NH, STR-SW. Single-Ended Slider. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1985-2024·2024-06-12

    Vascular Graft Swivel Rod Separation Recalled Due to Component Failure

    Atrium Medical Corporation is recalling ADVANTA VXT vascular grafts due to reports of separation between the Slider GDS Swivel Rod and Swivel Core, which could affect device function.

    Product
    ADVANTA VXT, 8X50, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V416000·2024-06-06

    RAM ProMaster vehicles recalled for missing side door beam and incorrect seating label

    Certain 2021-2024 RAM ProMaster vehicles lack a side door beam and have incorrect seating capacity information on the tire placard. These defects may reduce occupant protection in side-impact crashes and could result in improper vehicle loading.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V411000·2024-06-05

    Vermeer Recalls 2023 Vacuum Excavator Trailers Due to Frame Defect

    Vermeer is recalling 2023 LPSDT vacuum excavator trailers because the frame may bend or distort, potentially causing loss of stability and control while towing.

    Product
    VERMEER — VERMEER VACUUM EXCAVATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V410000·2024-06-05

    Wabash National Refrigerated Van Trailers Recalled for Base Rail Detachment Risk

    Wabash National Corporation is recalling certain 2024-2025 refrigerated van trailers because the base rails may not be bonded properly and can detach, reducing structural strength and increasing crash risk.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide