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.

401–425 of 2094

  • HighNHTSA·23V226000·2023-03-31

    2023 Forest River Cherokee Travel Trailers Safety Chain Recall

    Forest River is recalling certain 2023 Cherokee CKT36FBOP Travel Trailers because the safety chains may be insufficient for the Gross Vehicle Weight Rating listed on the federal placard, allowing the trailer to detach and increase crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V229000·2023-03-30

    Honda Recalls 2023 Civic Type R for Driver Seat Frame Welding Defect

    Honda is recalling 2023 Civic Type R vehicles because the driver's seat frame may not be welded properly, which could cause the seat cushion frame to break and increase injury risk in a crash.

    Product
    HONDA — HONDA CIVIC TYPE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1256-2023·2023-03-22

    Ambulance cot may separate due to insufficient epoxy in assemblies

    Stryker's Power-PRO 2 ambulance cots may separate at head or foot due to insufficient epoxy. Four affected units in NY and VA should be removed from service immediately.

    Product
    Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V130000·2023-02-27

    Tesla Recalls 2022-2023 Model Y Vehicles for Loose Seat Bolts

    Tesla is recalling 2022-2023 Model Y vehicles because second-row seat back frame bolts may not be securely tightened, potentially reducing seat belt performance.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V096000·2023-02-17

    Pierce Aerial Trucks Recalled for Basket Handrail Detachment Risk

    Pierce is recalling 2018-2023 Arrow XT, Enforcer, Velocity, and Impel 110-foot aerial trucks because the basket handrail may detach when the platform is extended.

    Product
    PIERCE — PIERCE VELOCITY, ENFORCER, ARROW XT, IMPEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E014000·2023-02-13

    Braun Recalls Child Seat Weldments Due to Improper Welds

    Braun Corporation is recalling child seat weldments for the BraunAbility Turny Seat because improper welds may cause anchors to detach in a crash.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V066000·2023-02-10

    Navistar Recalls 2022-2023 IC Bus CE and RE Models for Roof Defect

    Navistar is recalling 2022-2023 IC Bus CE and RE transit buses because roof panels may have insufficient joint strength, increasing injury risk in a crash.

    Product
    IC BUS — IC BUS CE, RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V065000·2023-02-10

    2022-2024 IC Bus School Buses Roof Panel Joint Strength Defect Recall

    Navistar is recalling certain 2022-2024 IC Bus school buses because roof panels may have insufficient joint strength and could separate during a crash, increasing injury risk. Dealers will add fasteners to secure the joints at no cost.

    Product
    IC BUS — IC BUS RESB, CESB, EV, CE SBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23C001000·2023-02-10

    Cybex Infant Car Seat Recall for Fraying Harness Adjustment Straps

    Columbus Trading-Partners USA is recalling specific Cybex infant car seats because the front harness adjustment strap webbing may fray, reducing strength and increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V061000·2023-02-09

    Motorhome Cooktops May Leak Gas and Create Fire Risk

    Forest River is recalling certain 2022-2023 Coachmen motorhomes with faulty cooktops. The burner tubes may fracture and leak gas, creating a fire hazard.

    Product
    COACHMEN — COACHMEN GALLERIA, BEYOND, NOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1000-2023·2023-01-25

    Medical X-ray equipment patient table footrests recalled due to detachment risk

    Siemens recalls four fluoroscopy and radiographic imaging equipment models worldwide because patient table footrests may detach during clinical use, potentially causing patient injury.

    Product
    AXIOM Luminos TF, AXIOM Iconos R100, AXIOM Iconos R200 and AXIOM Luminos dRF
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0984-2023·2023-01-25

    Cardinal Health Jackson-Pratt Channel Drains recalled for multiple performance defects

    Cardinal Health is recalling 2,277 Jackson-Pratt Channel Drains due to performance issues including lack of radiopacity, dull trocars, reduced flexibility, and broken tips. These defects may affect the drain's function and clinical performance.

    Product
    Cardinal Health Jackson-Pratt Channel Drain, 10 Fr, REF JP-2226
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0954-2023·2023-01-18

    Orthopedic Implant Cage Recalled for Incorrect Internal Material

    Specific lots of CoreLink FLXFIT 15 orthopedic implant cages contain stainless steel internal components instead of the specified titanium alloy. The 18 affected units were distributed nationwide.

    Product
    CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0880-2023·2023-01-11

    Shower/Commode Chair Recalled Due to Frame Folding Defect

    Altimate Medical is recalling the ActiveAid 922 Shower/Commode Chair because a manufacturing defect prevents the frame from folding properly and being secured by the frame strap in the folded position.

    Product
    ActiveAid 922, Shower/Commode Chair
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0764-2023·2022-12-28

    Baxter Revaclear 400 Dialyzers Recalled for Polyurethane Displacement

    Baxter Healthcare is recalling Revaclear 400 dialyzers because polyurethane displacement may cause blood leaks during dialysis treatment. Approximately 1.14 million units are affected worldwide.

    Product
    Revaclear 400 dialyzers. Indicated for treatment of chronic and acute renal failure by hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V938000·2022-12-16

    Mercedes-Benz Recalls 2019 AMG GT Models for Center Console Defect

    Mercedes-Benz is recalling 2019 AMG GT53 and GT63 vehicles because the center console may unlatch during a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT 63, AMG GT53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0337-2023·2022-12-14

    Liquid Oxygen System Devices Recalled Due to Weld Quality Issues

    Caire Inc. is recalling 70 CAIRE Liberator 45 liquid oxygen systems due to inconsistencies in weld penetration on the inner bottle's longitudinal weld seam discovered during an audit.

    Product
    CAIRE Liberator 45, MODEL 13262253, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0338-2023·2022-12-14

    FDA Class I Recall: CAIRE Liberator 30 Liquid Oxygen System Units

    Caire, Inc. is recalling five CAIRE Liberator 30 liquid oxygen system units due to weld defects on the inner bottle that could lead to device failure and loss of oxygen supply to dependent patients.

    Product
    CAIRE Liberator 30, MODEL 13337403, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0336-2023·2022-12-14

    Caire Liberator 45 Liquid Oxygen System Recalled for Weld Defects

    Caire, Inc. is recalling 10 CAIRE Liberator 45 liquid oxygen system units due to inconsistencies in weld penetration on the inner bottle discovered during an FDA audit.

    Product
    CAIRE Liberator 45, MODEL 13261699, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0339-2023·2022-12-14

    CAIRE Liberator 20 Liquid Oxygen System Recalled for Weld Defects

    Caire, Inc. is recalling CAIRE Liberator 20 liquid oxygen system units due to weld penetration inconsistencies discovered during an FDA audit. The manufacturing defect affects 3 units.

    Product
    CAIRE Liberator 20, MODEL 13256195, Liquid Oxygen System Unit
    Category
    Medical Device
    Distribution
    Distributed nationwide