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.

1576–1600 of 2056

  • SevereNHTSA·12V446000·2012-09-11

    Tracker Marine Recalls Mako 18 LTS Boats Due to Trailer Overload Risk

    Tracker Marine is recalling 2010-2013 Mako 18 LTS boat and trailer packages because the trailers may lack sufficient load capacity, increasing crash risk.

    Product
    TRACKER MARINE — TRACKER MARINE MAKO 18 LTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V423000·2012-08-30

    Altec Recalls 2011-2012 Digger Derrick Vehicles Due to Shaft Defect

    Altec Industries is recalling 2011-2012 Digger Derrick vehicles with PENGO extensions because a weld defect may cause the shaft to separate, risking injury or property damage.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12264·2012-08-30

    Shimano Recalls PRO VIBE Carbon Bicycle Handlebars Due to Fall Hazard

    Shimano is recalling about 67 PRO VIBE Carbon bicycle handlebars because they can break during riding, posing a fall hazard. No injuries have been reported.

    Product
    PRO VIBE Carbon bicycle handlebars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12255·2012-08-23

    Zest Garden Recalls Wilson & Fisher Bistro Sets Due to Fall Hazard

    Zest Garden is recalling Wilson & Fisher White Cast Bistro Sets because the chairs can break during normal use, posing a fall hazard.

    Product
    Wilson & Fisher White Cast Bistro Table and Chairs Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V411000·2012-08-21

    Altec Recalls 2008-2009 Aerial Devices Due to Boom Pivot Pin Defect

    Altec Industries is recalling 2008-2009 AH100 and AH85 aerial devices because improper welding of boom pivot pins could cause the boom to separate from the turntable.

    Product
    ALTEC — ALTEC AH100, AH85
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·12744·2012-08-16

    PBteen Recalls Beadboard Bunk Beds Due to Risk of Injury

    PBteen is recalling Beadboard Bunk Beds because the front upper horizontal panel can crack or break, posing a risk of injury.

    Product
    Beadboard Bunk Beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·12248·2012-08-16

    Gerber Bear Grylls Parang Machetes Recalled for Laceration Hazard

    Gerber is recalling Bear Grylls Parang Machetes because a weakness in the handle-blade connection can cause breakage, posing a laceration risk.

    Product
    Gerber® Bear Grylls Parang Machetes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2155-2012·2012-08-15

    Stryker Luxor Retractor Base Recalled Due to Blade Disassembly

    Stryker Spine is recalling 30 Luxor Retractor Base devices because blades may disassemble from the base, causing the retractor to collapse during use.

    Product
    LUXOR RETRACTOR BASE; Catalog Number: 48250030; Manufactured by: STRYKER Spine SAS; Z.I MARTICOT-33610-CESTAS-FRANCE; Distributed in the USA by: Stryker Spine. 2 Pearl Ct. Allendale, NJ 07401. Provides access to the thoracic and lumbar spine from a posterior approach via a sma
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2165-2012·2012-08-15

    Smith & Nephew TWINFIX Ultra Ti Suture Anchor Recall for Breakage Risk

    Smith & Nephew is recalling 913 units of TWINFIX Ultra Ti Suture Anchors because the distal part may break during insertion into bone.

    Product
    Smith & Nephew 5.5 mm TWINFIX Ultra Ti Suture Anchor with two #2 ULTRABRAID sutures (blue, blue-COBRAID) with Needles Product Usage: intended for use for the reattachment of soft tissue to bone Part Number: 72202618
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2166-2012·2012-08-15

    Smith & Nephew TWINFIX Ultra Ti Anchor Recall for Breakage Risk

    Smith & Nephew is recalling 4,661 units of TWINFIX Ultra Ti Anchors because the distal part may break during insertion into bone.

    Product
    Smith & Nephew 5.5 mm TWINFIX Ultra Ti Anchor with two #2 sutures(white, COBRAID-blue), sterile Part Number: 72202895 Product Usage: intended for use for the reattachment of soft tissue to bone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V383000·2012-08-03

    Altec Wood Chippers Recalled for Frame Cracks and Injury Risk

    Altec Environmental Products is recalling specific wood chippers because cracks in the frame could lead to personal injury or property damage.

    Product
    ALTEC — ALTEC DC1217, DC1317HP, DC1317
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V373000·2012-08-02

    Toyota Recalls RAV4 and Lexus HS 250h for Rear Suspension Defect

    Toyota is recalling 2006-2011 RAV4 and 2010 Lexus HS 250h vehicles because rear tie rods may fail, causing loss of vehicle control.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4, HS 250 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2077-2012·2012-08-01

    Anspach Effort Recalls Sterile Bone Cutting Burrs Due to Breakage Risk

    The Anspach Effort, Inc. is recalling specific sterile bone cutting burrs because the cutter may come apart during use.

    Product
    .***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine and cranium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2033-2012·2012-07-25

    Stryker AVS Navigator Trials Recalled for Shaft Failure

    Stryker Spine is recalling AVS Navigator Trials because the shaft may fail at the junction of the trial head.

    Product
    Stryker AVS Navigator Trials 6mm-15mm Manufactured by: Stryker Spine SAS Z.1 Marticot-33610-Cestas -France +33 (0) 5.57.97.06.30 http;//www.stryker.com Distributed in the USA by Stryker Spine 2 Pearl Court. Allendale NJ 07401-1677 USA +1-201-780-8000 Cestas France 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V358000·2012-07-24

    Daimler Recalls 2013 Thomas Built School Buses for Front Axle Defect

    Daimler Trucks North America is recalling two 2013 Thomas Built Saf-T-Liner C2 school buses due to a front axle machining error that could cause wheel separation and loss of control.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1980-2012·2012-07-18

    Zimmer Recalls Pathfinder NXT Fixed Percutaneous Rod Holder Due to Cracking

    Zimmer, Inc. is recalling Pathfinder NXT Fixed Percutaneous Rod Holders because the tip may crack or break during surgery.

    Product
    Pathfinder NXT Fixed Percutaneous Rod Holder, Part numbers 3573-1 (angle handle) , Stainless Steel / Silicone Rubber, Rx only, non sterile. Product Usage: The rod is held by the instrument for inserting and guiding into the screw heads via percutaneous delivery during minimal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1981-2012·2012-07-18

    Zimmer Recalls Pathfinder NXT Fixed Percutaneous Rod Holder Due to Cracking

    Zimmer, Inc. is recalling the Pathfinder NXT Fixed Percutaneous Rod Holder because the tip may crack or break during surgery.

    Product
    Pathfinder NXT Fixed Percutaneous Rod Holder, Part numbers 3573-2 (straight handle) Stainless Steel / Silicone Rubber, Rx only, non sterile. Product Usage: PathFinder NXT is a minimally invasive pedicle screw system. The PathFinder NXT System consists of various screws and ro
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1982-2012·2012-07-18

    Stryker Definition PM Femoral Hip Stem Recalled for PMMA Coating Cracking

    Stryker Howmedica Osteonics is recalling 16,913 Definition PM Femoral Hip Stems due to potential cracking of the PMMA coating. The devices were distributed nationwide.

    Product
    Stryker Orthopaedics, Definition PM Femoral Hip Stem Catalog Numbers 6265-3-099 through 6265-3-107. Howmedica Osteonics Corp. 325 Corporate Drive, Mahwah, NJ 07430. A subsidiary of Stryker Corp. Stryker France, ZAC Satorlas Green Pusignan, Av De Satolas Green 69881 Meyzeiu, Ced
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·12227·2012-07-18

    Samuel Lawrence Furniture Recalls Bordeaux Sleigh Beds Due to Fall Hazard

    Samuel Lawrence Furniture is expanding a recall of Bordeaux Collection sleigh beds because the headboard or footboard hardware can loosen or detach, posing a fall hazard.

    Product
    Full- and Twin-Size Bordeaux Collection Bed Frames
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1901-2012·2012-07-11

    CareFusion Infant Y Connector Recall Due to Spontaneous Cracking

    CareFusion is recalling AirLife Infant Patient Y Connectors because the adapter may crack, causing a leak that reduces the air volume delivered to ventilated patients.

    Product
    AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector; an Rx device for single patient use; 30 connectors per box; CareFusion, 22745 Savi Ranch Parkway, Yorba Linda, CA 92887 USA, Made in Mexico Respiratory breathing circuits are used with a ventilator wh
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·12V306000·2012-06-29

    Isuzu Recalls Amigo and Rodeo Sport for Rear Suspension Corrosion

    Isuzu is recalling 1998-2002 Amigo and Rodeo Sport vehicles in 21 states and D.C. due to rear suspension corrosion that may increase crash risk.

    Product
    ISUZU — ISUZU RODEO SPORT, AMIGO
    Category
    Vehicle
    Distribution
    Distributed nationwide