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.

401–425 of 2056

  • SevereNHTSA·21V437000·2021-06-09

    Karavan Recalls 2021 Move I 1500 Long Trailers Due to Axle Weld Defect

    Karavan is recalling 2021 Move I 1500 Long trailers because improperly welded wheel spindles can break, causing the wheel to detach and increasing crash risk.

    Product
    KARAVAN — KARAVAN MOVE I 1500 LONG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1687-2021·2021-06-02

    James Leckey MyWay Walker Chassis Recalled Due to Weld Failure

    James Leckey Design Ltd is recalling 2,719 MyWay Walker Chassis units because weld failures caused casters to detach from the rear legs.

    Product
    MyWay Walker Chassis - Product Usage: is intended for use by children already using a supportive walking device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21751·2021-05-27

    Umbrosa Pool and Patio Umbrellas Recalled Due to Arm Breakage Hazard

    Umbrosa is recalling about 250 pool and patio umbrellas because the arm can break at the elbow while in use, posing an injury hazard.

    Product
    Umbrosa umbrellas equipped with the Umbrosa Evolution Arm/Holder
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21E047000·2021-05-21

    Lippert Recalls Hehr 6400 Series RV Windows Due to Adhesive Failure

    Lippert is recalling Hehr 6400 Series windows for recreational vehicles because the adhesive may fail, causing the vent to detach and increasing crash risk.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21137·2021-05-19

    Cheyenne Mainstay Folding Chairs and Barstools Recalled for Fall Hazard

    Cheyenne Products is recalling about 795,000 Mainstay folding chairs and barstools because a weld can break, posing a fall hazard. Consumers should stop using them and contact Cheyenne for a refund.

    Product
    Cheyenne Products Mainstay folding metal padded chairs and barstools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21747·2021-05-13

    Leisure Time Recalls Brutus Swing Sets Due to Injury Hazard

    Leisure Time Products is recalling about 9,000 Brutus metal swing sets because the swing hanger attachment can fail, causing the swing to fall.

    Product
    Backyard Discovery Big Brutus, Little Brutus and Mini Brutus metal A-frame swing sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E045000·2021-05-12

    Thule Recalls Rooftop Tents Due to Shell Cracking Risk

    Thule is recalling specific Tepui Hybox rooftop tents because the shell may crack at the mounting points, creating a road hazard.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1514-2021·2021-05-05

    Donjoy Ultrasling Pro AB Arm Sling Recalled for Failed Rivet

    DJ Orthopedics is recalling Donjoy Ultrasling Pro AB arm slings due to a failed rivet at the chafe tab.

    Product
    DONJOY REF:11-0473-9 ULTRASLING PRO AB, UNIVERSAL, Rx ONLY, UDI: (01)00190446683681 - Product Usage: intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1512-2021·2021-05-05

    Donjoy Ultrasling Pro Arm Sling Recalled for Failed Rivet

    DJ Orthopedics is recalling Donjoy Ultrasling Pro arm slings because a rivet at the chafe tab failed, potentially compromising the device's ability to immobilize the arm.

    Product
    DONJOY REF:11-0471-9 ULTRASLING PRO ER/IR 15, UNIVERSAL, Rx ONLY, UDI: (01) 00190446683667 - Product Usage: intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1513-2021·2021-05-05

    DJ Orthopedics Recalls Ultrasling Pro Arm Sling Due to Failed Rivet

    DJ Orthopedics is recalling Ultrasling Pro arm slings because a rivet at the chafe tab failed. The defect could compromise the device's ability to immobilize the arm.

    Product
    DONJOY REF:11-0472-9 ULTRASLING PRO ER/IR 30, UNIVERSAL, Rx ONLY, UDI: (01)00190446683674 - Product Usage: intended for medical purposes to immobilize the arm, by means of a fabric band suspended from around the neck.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21E037000·2021-04-29

    Full Vision Recalls Rogers Brothers Rear Impact Guards Due to Weak Steel

    Full Vision is recalling Rogers Brothers Rear Impact Guards because the steel may not meet specifications, potentially reducing strength and increasing injury risk in crashes.

    Product
    STRUCTURE:BODY:BUMPERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V254000·2021-04-12

    Palfinger Roll-Off and Hoist Recall for Tarp Arm Fatigue Failure

    Omaha Standard is recalling 2019-2021 Palfinger American Roll-Off, Cable Hoist, and Hook Lift units because welded gusset fatigue may cause tarp arms to break.

    Product
    PALFINGER — PALFINGER HOOK LIFT, AMERICAN ROLL OFF, CABLE HOIST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1228-2021·2021-03-17

    CervAlign Anterior Cervical Plate System Recall for Locking Mechanism Failure

    RTI Surgical is recalling CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 60mm Material Number: 66-460 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1209-2021·2021-03-17

    RTI Surgical Recalls CervAlign Anterior Cervical Plate System Due to Locking Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 1 Level, 20mm Material Number: 66-120 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1213-2021·2021-03-17

    CervAlign Anterior Cervical Plate System Recalled for Locking Mechanism Failure

    RTI Surgical is recalling CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 28mm Material Number: 66-228 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1224-2021·2021-03-17

    CervAlign Anterior Cervical Plate System Recalled for Locking Mechanism Failure

    RTI Surgical is recalling specific CervAlign Anterior Cervical Plate Systems because the locking mechanism may disassociate, requiring revision surgery.

    Product
    CervAlign Anterior Cervical Plate System-Cervalign, 3Level, 54mm Material Number: 66-354 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of t
    Category
    Medical Device
    Distribution
    Distributed nationwide