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.

1426–1450 of 2094

  • SevereNHTSA·16V227000·2016-04-20

    Starcraft Bus Recalls 2015-2016 Prodigy and Quest School Buses

    Forest River is recalling 2015-2016 Starcraft Prodigy and Quest school buses because seats may separate from the base frame due to bolt failure.

    Product
    STARCRAFT BUS — STARCRAFT BUS QUEST, PRODIGY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1393-2016·2016-04-20

    RTI Surgical Streamline OCT Final Driver Recalled for Fracture Risk

    RTI Surgical is recalling Streamline OCT Final Drivers due to reduced mechanical strength that may cause the tip to fracture during use.

    Product
    RTI Surgical Streamline Occipito-Cervico-Thoracic (OCT) Final Driver, Common Name: Screw Driver
    Category
    Medical Device
    Distribution
    13 states
  • LowFDA (Devices)·Z-1350-2016·2016-04-20

    Siemens Recalls One CT System Due to Front Cover Welding Defect

    Siemens is recalling one SOMATOM Definition AS CT system because a front cover weld defect could cause a bolt to break during service, though no clinical risk exists.

    Product
    SOMATOM Definition AS, a family of CT systems intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission dta from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1327-2016·2016-04-13

    Synthes Recalls Titanium Low Profile Neuro Screws Due to Thread Defect

    Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, potentially compromising the device's structural integrity.

    Product
    Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and sel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V214000·2016-04-13

    Hillsboro Aluminum Utility Trailer Recall for Axle Hardware Defect

    Hillsboro is recalling 2016 aluminum utility trailers because improperly installed axle hardware may cause the axle to shift, increasing crash risk.

    Product
    HILLSBORO — HILLSBORO ALUMINUM UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1326-2016·2016-04-13

    Synthes Recalls Titanium Low Profile Neuro Screws Due to Thread Defect

    Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, which may affect the device's structural integrity.

    Product
    Titanium Low Profile Neuro Screw, Self Drilling, 3mm, part numbers: 400.833, 400.833E Product Usage: The Low Profile Neuro Plating System is intended for use in selective trauma of the midface and craniofacial skeleton; craniofacial surgery; reconstructive procedures; and sel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1261-2016·2016-04-06

    ICU Medical Recalls I.V. Infusion Sets with Potential Leak

    ICU Medical is recalling 400 units of I.V. infusion administration sets because the connection between the drip chamber and ChemoLock port may develop a leak.

    Product
    31" (79 cm) Appx. 3.4 ml, 20 Drop Admin Set w/ Integrated ChemoLock Port Drip Chamber, Spiros, Bag Hanger, Item No. SL3011 sterile devices intended for the infusion and withdrawal of fluids.
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·16V191000·2016-04-05

    Nova Bus Recalls 2010-2015 LFS Transit Buses for Seat Belt Defect

    Nova Bus is recalling 2010-2015 LFS transit buses because missing welds on seat J-Brackets may allow seat belt anchorages to separate, increasing injury risk in a crash.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V180000·2016-03-30

    Starcraft RV Recalls 2016 Launch Ultra Lite Trailers Due to Step Defect

    Starcraft RV is recalling 26 model year 2016 Launch Ultra Lite trailers because entry steps may have been installed with improper bolts, posing a fall risk.

    Product
    STARCRAFT RV TT — STARCRAFT RV TT LAUNCH ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V176000·2016-03-29

    Forest River Georgetown RVs Recalled for Missing Emergency Egress Window

    Forest River is recalling 2015-2017 Georgetown RVs because a vented window was installed instead of a required secondary egress window, posing a risk of entrapment.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1188-2016·2016-03-23

    Richard Wolf Vesa 75/100 Adaptation Recalled for Missing Rivets

    Richard Wolf Medical Instruments Corp. is recalling 108 Vesa 75/100 adaptations with rotation because monitor mounts may be missing riveting.

    Product
    The Vesa 75/100 adaptation with rotation is an accessory to a surgical camera intended to be used to record operative procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V158000·2016-03-17

    Jayco Recalls 2016 White Hawk Travel Trailers Due to Axle Defect

    Jayco is recalling 10 model year 2016 White Hawk travel trailers because they were built with axles rated for 3000 lbs instead of the required 3500 lbs, which may affect handling.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER WHITE HAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V155000·2016-03-16

    Winnebago Recalls 2015-2016 RVs for Improperly Torqued Hitch Bolts

    Winnebago is recalling certain 2015-2016 Adventurer and Itasca Suncruiser vehicles because hitch bolts were not properly torqued, which could cause the hitch to detach and increase crash risk.

    Product
    WINNEBAGO — WINNEBAGO, ITASCA ADVENTURER, SUNCRUISER, COMMERCIAL VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V154000·2016-03-16

    Terex Recalls Aerial Devices Due to Suspension Air Bag Defect

    Terex is recalling 2015-2016 aerial devices and digger derrick lifts because the suspension circuit can inflate air bags, lifting outriggers and increasing injury risk.

    Product
    TEREX — TEREX TM125, HRX, C5000, C6000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1068-2016·2016-03-16

    Bard Denali Filter Delivery System Recalled for Cracking Stop Cocks

    Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.

    Product
    Denali Filter-Jugular/Subclavian Delivery System Product Code: DL900J/DL950J; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1069-2016·2016-03-16

    Bard Denali Filter Delivery Systems Recalled for Cracking Stop Cocks

    Bard Peripheral Vascular is recalling Denali Filter Delivery Systems because stop cocks may crack.

    Product
    Denali Filter-Femoral Delivery System Product Code: DL900F/DL950F; Indicated for use in the prevention of recurrent pulmonary embolism via placement in the vena cava.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V144000·2016-03-09

    Van Hool Motor Coaches Recalled for Potential Seat Belt Anchor Separation

    Van Hool is recalling specific motor coaches because missing welds on seat brackets could allow the driver's seat belt anchorage to separate during a crash.

    Product
    VAN HOOL — VAN HOOL C2045, T2145, TD925, TX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V132000·2016-03-04

    Haulmark Motorcoach Recall for Unstable Entry Steps

    Universal Trailer is recalling 2007-2010 Haulmark Motorcoaches because a bolt may fracture, causing entry steps to become unstable and increasing injury risk.

    Product
    HAULMARK — HAULMARK MOTORCOACH
    Category
    Vehicle
    Distribution
    Distributed nationwide