The Recall Desk

Hazard

Structural Failure recalls

2,074 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
2,074
Critical
11
Severe
1,064
Most recent
2026-10-29

Of the 2,074 structural failure recalls we have scored against our rubric, 11 (1%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,064 (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.

451–475 of 2074

  • SevereNHTSA·21V092000·2021-02-18

    Trail King Recalls 2021 TKSA Trailers Due to Frame Crack Risk

    Trail King is recalling 2021 TKSA trailers because a cross member in the slide pan frame may crack and detach, increasing crash risk.

    Product
    TRAIL KING — TRAIL KING TKSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1072-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 483 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, 1/6f Straight Catheter, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-1073-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 863 TLAB Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19, 1/19 GA Flexcore Biopsy Needle, 7F Introducer Sheath W/Curved Metal Stiffener, Tissue Removal Swabs, 5F Straight Catheter, 5F Curved Catheter, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-1076-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems Due to Sheath Separation

    Argon Medical Devices is recalling 1,759 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18C, 1/18 GA Flexcore Biopsy Needle, 1/7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, 1/5f straight catheter, 1/5F Curved Catheter Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-1077-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 583 Transjugular Liver Biopsy Systems due to a manufacturing error that may cause the sheath to separate during use.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18N, 1/18 GA Flexcore Biopsy Needle, 1/7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • SevereFDA (Devices)·Z-1075-2021·2021-02-17

    Argon Medical Devices Recalls Transjugular Liver Biopsy Systems

    Argon Medical Devices is recalling 247 Transjugular Liver Biopsy Systems because a manufacturing error may cause the sheath to separate during use, potentially requiring surgical intervention.

    Product
    Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19S, 1/19 GA Flexcore Biopsy Needle, 1/7F Introducer Sheath W/Curved Metal Stiffener, 4/Tissue Removal Swabs, 1/5f straight catheter, Sterile EO,
    Category
    Medical Device
    Distribution
    46 states
  • HighCPSC·21721·2021-02-11

    Rep Fitness Recalls Strap Safety Brackets Due to Injury Hazard

    Rep Fitness is recalling approximately 1,940 Strap Safety Brackets because improperly welded brackets may detach when weight is dropped, posing an injury risk.

    Product
    Strap Safety Brackets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21076·2021-02-10

    Edsal Recalls 2.2 Million Heavy Duty Steel Shelving Units

    Edsal is recalling 2.2 million shelving units because they may fail to support the advertised 800-pound load, posing an injury hazard.

    Product
    Muscle Rack Heavy Duty Steel Shelving Units
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E007000·2021-02-01

    Howmet Aerospace Recalls Alcoa High Polish Aluminum Wheels

    Howmet Aerospace is recalling specific Alcoa High Polish Aluminum Wheels that may bend or break under load, increasing the risk of a crash.

    Product
    WHEELS:RIM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E094000·2020-12-28

    Summit Racing 6-Ton Jack Stands Recalled Due to Ratchet Bar Failure Risk

    Autosales Inc. is recalling Summit Racing 6-Ton Jack Stands because the ratchet bar may fail, allowing the vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.

    Product
    EQUIPMENT:MECHANICAL:ACCESSORY SCISSOR/SCREW/BOTTLE JACK/LIFT:STAND recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0579-2021·2020-12-23

    DePuy Synthes 14.0MM Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 14.0MM Reamer Heads for RIA 2 due to breakage rates exceeding expectations, which can cause tissue and bone damage.

    Product
    DePuy Synthes 14.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.024S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0581-2021·2020-12-23

    DePuy Synthes 15.0mm Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 15.0mm Reamer Heads for RIA 2 due to breakage rates exceeding expectations, which can cause tissue or bone damage.

    Product
    DePuy Synthes 15.0MM REAMER HEAD FOR RIA 2 STERILE -Orthopedic manual surgical instrument Part Code: 03.404.026S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E093000·2020-12-23

    Autosales Recalls Summit Racing 3-Ton Jack Stands Due to Ratchet Bar Failure

    Autosales is recalling Summit Racing 3-Ton Jack Stands because the ratchet bar may fail, allowing a vehicle to fall. Owners should stop using the stands and contact Autosales for a refund.

    Product
    EQUIPMENT:MECHANICAL:ACCESSORY SCISSOR/SCREW/BOTTLE JACK/LIFT:STAND recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0587-2021·2020-12-23

    DePuy Synthes 18.0mm Reamer Head Recalled for Breakage and Tissue Damage

    Synthes (USA) Products LLC is recalling DePuy Synthes 18.0mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.

    Product
    DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.032S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E091000·2020-12-11

    Ohlins Recalls Front Struts for Porsche 911 Models Due to Pin Breakage Risk

    Ohlins is recalling front struts for specific Porsche 911 models because the strut pin may break during maximum steering, potentially causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE 911 CARRERA, 911 TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21036·2020-11-25

    Santa Cruz Recalls 2020 Aluminum Bicycles Due to Frame Buckling Risk

    Santa Cruz Bicycles is recalling about 2,900 model year 2020 aluminum frames because thermal damage can cause them to bend or buckle, posing a fall hazard.

    Product
    Model Year 2020 Aluminum Santa Cruz and Juliana Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E086000·2020-11-16

    Aries Recalls Tow Hitches Due to Potential Structural Failure

    Aries Industries is recalling certain Class 3 and Class 4 tow hitches because they may not support rated weights, risking hitch failure and vehicle separation.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21025·2020-11-10

    Salsa Cutthroat Bicycles Recalled Due to Fork Crack Injury Hazard

    Quality Bicycle Products is recalling Salsa Cutthroat bicycles because the fork legs can crack or break, posing a fall hazard to riders.

    Product
    Salsa Cutthroat Bicycles and Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide