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.

1551–1575 of 2094

  • SevereNHTSA·15E038000·2015-05-12

    Fleetline Recalls Fender Brackets Due to Insufficient Welds

    Fleetline is recalling specific Nu-Line and Fleetline fender brackets and kits due to insufficient welds that may cause fender separation.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V267000·2015-05-08

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon Trucks for Seat Defect

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon trucks because seat frame hooks may not be properly attached, increasing injury risk in a crash.

    Product
    GMC — GMC, CHEVROLET CANYON, COLORADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V265000·2015-05-07

    Thor Motor Coach Recalls 2016 Hurricane and Windsport Motorhomes for Seat Defect

    Thor Motor Coach is recalling 2016 Hurricane and Windsport motorhomes because the co-pilot seat mounting area may not be properly reinforced, increasing injury risk in a crash.

    Product
    THOR MOTOR — THOR MOTOR, THOR MOTOR COACH HURRICANE, WINDSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1520-2015·2015-05-06

    AmTryke Model 1424 Hand Cycle Recalled for Cracked Frames

    Amtryke LLC is recalling 53 Model 1424 Community Cruiser Hand Cycles due to complaints of cracked frames. The recall covers units distributed nationwide to 18 states.

    Product
    AmTryke Model 1424 Community Cruiser Hand Cycle. Therapeutic tricycle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2015·2015-05-06

    Pega Medical Recalls Female Driver Instruments for Orthopedic Procedures

    Pega Medical Inc. is recalling 9 Female Driver instruments used in orthopedic procedures because the hexagonal tip is 0.06 mm under specifications, which may lead to breakage.

    Product
    Female Driver, Part number FDr101, instrument used for the insertion of the Fassier-Duval IM Telescopic System. For orthopedic procedures. This instrument is included in the Fassier-Duval IM Telescopic System instrument tray. This instrument is marked with the catalogue num
    Category
    Medical Device
    Distribution
    4 states
  • SevereNHTSA·15V264000·2015-05-05

    Eldorado Amerivan 10 Recall for Rear Shock Absorber Separation Risk

    Eldorado is recalling 2012-2015 Amerivan 10 vehicles because the rear shock absorber may separate, potentially damaging fuel lines and causing a fire.

    Product
    ELDORADO — ELDORADO AMERIVAN 10
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1498-2015·2015-04-29

    Wright Medical Recalls Crosscheck Plating System Due to Specification Defects

    Wright Medical Technology is recalling 100 units of Crosscheck Plating Systems because dimensional specifications are out of tolerance, posing a risk of intraoperative malfunction.

    Product
    CROSSCHECK(R) Plating system, Utility Plate, 6-Hole, REF CCP-UTN6. Orthopedic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V239000·2015-04-22

    Polaris Recalls 2009-2010 GEM eLXD Vehicles Due to Frame Weld Cracks

    Polaris is recalling 2009-2010 GEM eLXD hybrid electric vehicles because frame welds may crack, potentially causing the frame to fall and stop the vehicle suddenly.

    Product
    GEM — GEM ELXD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V240000·2015-04-22

    Toyota Recalls 2015 Sienna Minivans Due to Trim Panel Clip Defect

    Toyota is recalling 387 model year 2015 Sienna minivans because a reused trim panel clip may detach during airbag deployment, posing an injury risk to occupants.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1442-2015·2015-04-22

    Baylis Medical Recalls ProTrack Microcatheter Due to Circumferential Shaft Defects

    Baylis Medical Corp is recalling two lots of ProTrack Microcatheters due to potential circumferential defects along the device shaft.

    Product
    ProTrack Microcatheter; Product Usage: The ProTrack Microcatheter is a sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V236000·2015-04-21

    Toyota Recalls 2015 Siennas for Potential Trim Panel Detachment Risk

    Toyota is recalling 2015 Siennas with dealer-installed entertainment systems because a reused clip may allow a trim panel to detach during airbag deployment.

    Product
    TOYOTA — TOYOTA SIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V228000·2015-04-17

    Toyota Recalls 2015 Scion tC for Rear Suspension Tightening Defect

    Toyota is recalling 114 model year 2015 Scion tC vehicles because rear suspension components may not have been properly tightened, increasing the risk of a crash.

    Product
    SCION — SCION TC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V209000·2015-04-07

    Highland Ridge RV Recalls 2015-2016 Trailers Due to Slide Room Defect

    Highland Ridge RV is recalling 238 model year 2015-2016 travel and fifth wheel trailers because slide room screws may fail, allowing the room to extend while driving and increasing crash risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW JOURNEYER, LIGHT, MESA RIDGE, ROAMER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V203000·2015-04-06

    Forest River Recalls Fifth Wheel and Travel Trailers Due to Slide Room Defect

    Forest River is recalling specific 2015-2016 fifth wheel and travel trailers because slide room screws may fail, allowing the room to extend while driving and increasing crash risk.

    Product
    TRACER — TRACER, PURSUIT, GEORGETOWN TRT3200BHT, 31BD, GT335, CAF3825FL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1324-2015·2015-04-01

    Titan Spine Recalls TCS Straight Hexalobe Drivers Due to Tip Shearing

    Titan Spine, LLC is recalling 26 Endo TCS Driver Straight Hexalobe #6 units because the tips sheared off during use in patients with dense bones.

    Product
    Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004, Non-Sterile, Manufactured by Titan Spine, LLC. Endo TCS driver is one of the instruments within the surgical tray for use with the Interbody Fusion Device(IBD).
    Category
    Medical Device
    Distribution
    18 states
  • SevereNHTSA·15V191000·2015-03-31

    Thor Motor Coach Recalls 2015 Siesta and Citation Motorhomes

    Thor Motor Coach is recalling 2015 Siesta and Citation motorhomes because an incorrectly installed door component may make doors harder to open after a crash.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH SIESTA, CITATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V187000·2015-03-30

    Coachmen Prism Recalled for Incorrect Door Component Installation

    Forest River is recalling 2015 Coachmen Prism RVs because an incorrectly installed door component may make doors harder to open after a crash.

    Product
    COACHMEN — COACHMEN PRISM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1288-2015·2015-03-25

    Ossur LP Rotate Foot System Recalled for Insecure Assembly

    Ossur H / F is recalling LP Rotate Foot System prosthetic devices because short threads on the shock module may cause it to detach, leading to falls.

    Product
    LP Rotate Foot System prosthetic device for fitting lower extremity amputations. -Low profile foot module with adjustable shock absorber and rotation with progressive stiffening -Build height: with male pyramid adapter 145 - 153mm (5 11/16 - 6 ) with female pyramid adapte
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V174000·2015-03-25

    Pierce Recalls 2015 Vehicles Due to Rear Leaf Spring Spacer Defect

    Pierce Manufacturing is recalling 2015 Saber, Enforcer, Impel, and Velocity vehicles because the rear leaf spring spacer block may crack, posing a crash risk.

    Product
    PIERCE — PIERCE IMPEL, ENFORCER, SABER, VELOCITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1251-2015·2015-03-18

    Philips DuraDiagnost X-Ray System Recalled for Installation Defects

    Philips Medical Systems is recalling 71 DuraDiagnost X-Ray systems worldwide due to improper installation risks that could cause equipment to fall or float.

    Product
    Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·15V141000·2015-03-11

    BMW Recalls Motorcycles Due to Rear Wheel Mounting Flange Crack Risk

    BMW is recalling specific 2005-2011 motorcycles because the rear wheel mounting flange may crack if bolts are over-tightened, potentially causing the wheel to detach.

    Product
    BMW — BMW R 1200 ST, HP2 ENDURO, K 1300 S, R 1200 GS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1221-2015·2015-03-11

    Halyard Health Recalls KimVent Closed Suction Systems Due to Air Leak Defect

    Halyard Health is recalling KimVent Closed Suction Systems for Adults because a hole or crack may cause air to leak. The recall affects 5 cases distributed to specific US states and Japan.

    Product
    KimVent Closed Suction System for Adults, Double Swivel Elbow, 14 Fr. Sterile, Distributed by Kimberly Clark Global Systems, LLC.
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·15V135000·2015-03-09

    Winnebago Recalls 2015 RVs Due to Door Opening Defect

    Winnebago is recalling 2015 ERA, View, and Itasca Navion vehicles because an incorrectly installed door component may make doors harder to open after a crash.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA VIEW, ERA, NAVION
    Category
    Vehicle
    Distribution
    Distributed nationwide