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.

751–775 of 2094

  • SevereNHTSA·19V901000·2019-12-18

    Forest River Recalls 2020 Motorhomes Due to Trailer Hitch Bolt Issue

    Forest River is recalling 2020 Georgetown and FR3 motorhomes because improperly tightened trailer hitch bolts may loosen, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN, FR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0672-2020·2019-12-18

    Conformis Recalls iTotal CR Knee Replacement System Due to Fit Issues

    Conformis, Inc. is recalling the iTotal CR Knee Replacement System because the polyethylene inserts did not securely fit into the cobalt chrome tray implant.

    Product
    iTotal CR Knee Replacement System Model Number: TCR-111-1111-010102 - Product Usage: The iTotal CR Knee Replacement System is intended for use as a total knee replacement in patients with knee joint pain and disability whose conditions cannot be solely addressed by the use of a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V894000·2019-12-16

    Maintainer Recalls 2019 Custom Body Heavy Rescue Vehicle for Shock Defect

    Maintainer is recalling one 2019 Custom Body Heavy Rescue vehicle because front shocks may separate, potentially causing a steering fluid leak and loss of power steering assist.

    Product
    MAINTAINER — MAINTAINER CUSTOM BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V891000·2019-12-13

    Forest River Recalls 2020 Motorhomes Due to Trailer Hitch Bolt Issue

    Forest River is recalling 2020 Georgetown and FR3 motorhomes because trailer hitch bolts may not be properly tightened, posing a crash risk while towing.

    Product
    FOREST RIVER — FOREST RIVER FR3, GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V879000·2019-12-11

    Volkswagen Recalls 2019 Jetta and Golf Models for Wheel Bearing Defect

    Volkswagen is recalling 2019 Jetta GLI, Golf Alltrack, and Golf GTI vehicles because improperly machined front wheel bearings may cause excessive stress, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA, GOLF ALLTRACK, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0538-2020·2019-12-11

    GE Healthcare Recalls Giraffe OmniBed Infant Warmers Due to Latch Defect

    GE Healthcare is recalling Giraffe OmniBed infant warmers because bedside panels and portholes may appear closed without being latched, posing a risk of patient falls.

    Product
    Giraffe OmniBed infant warmer
    Category
    Medical Device
    Distribution
    0 states
  • SevereCPSC·20035·2019-12-06

    Trek Recalls Super Commuter+ Electric Bicycles Due to Fall Hazard

    Trek is recalling about 2,840 Super Commuter+ 8S electric bicycles because a front fender bolt can unthread, causing the wheel to detach and posing a fall hazard.

    Product
    Trek Super Commuter+ 8S
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V867000·2019-12-06

    Mercedes-Benz Recalls 2020 GLE 450 for Third-Row Headrest Defect

    Mercedes-Benz is recalling one 2020 GLE 450 4MATIC because third-row headrests may not hold in place, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V865000·2019-12-05

    Honda Recalls 2019-2020 CR-V for Rear Subframe Bolt Defect

    Honda is recalling 2019-2020 CR-V vehicles because improperly manufactured rear subframe bolts may loosen, allowing the subframe to separate and increasing crash risk.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0545-2020·2019-12-04

    Abbott Alinity ci Level Sensor Bulk Solution Recalled for Reliability Issues

    Abbott is recalling Alinity ci Level Sensor Bulk Solution kits due to potential cracks caused by environmental stress, which may affect reliability.

    Product
    Accessory kit, Alinity c containing Alinity ci Level Sensor, Bulk Solution
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0544-2020·2019-12-04

    Abbott Alinity i Accessory Kit Recalled for Potential Sensor Cracks

    Abbott is recalling Alinity i accessory kits because environmental stress may cause cracks in the bulk solution level sensor.

    Product
    Accessory kit, Alinity i containing Alinity ci Level Sensor, Bulk Solution
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0509-2020·2019-11-27

    Applied Medical Recalls Epix Electrosurgical Probes Due to Tip Insulation Shifting

    Applied Medical Resources Corp is recalling Epix Electrosurgical Probes because the tip insulation may shift unintentionally. The recall affects 28 units in the US and 112 units internationally.

    Product
    Epix Electrosurgical Probes with Smoke Evacuation, Angled L-Hook Tip, 5mm x 42 cm REF CW002 QTY: 1 - Product Usage: The Epix Electrosurgical Probe with Smoke Evacuation is intended to deliver energy from an independent monopolar electrosurgical generator to cut and coagulate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V848000·2019-11-26

    Forest River Recalls 2020 XLR Boost Trailers Due to Axle Defect

    Forest River is recalling 2020 XLR Boost trailers because an undersized axle and tire combination may cause the trailer to be overloaded, increasing the risk of a crash.

    Product
    FOREST RIVER — FOREST RIVER XLR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V842000·2019-11-22

    TransTech School Buses Recalled for Roof Hatch Handle Defect

    Transportation Collaborative is recalling 2019-2020 TransTech school buses because the roof hatch handle may break, preventing emergency exit.

    Product
    TRANS TECH — TRANS TECH SST, CST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V825000·2019-11-18

    Ducati Recalls 2018 Multistrada 1260 Motorcycles Due to Side Stand Defect

    Ducati is recalling 2018 Multistrada 1260 motorcycles because the side stand may be improperly welded. If the stand breaks, the motorcycle may fall over, increasing injury risk.

    Product
    DUCATI — DUCATI MULTISTRADA 1260
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V823000·2019-11-18

    BMW Recalls 2015-2019 X6 Models for Child Seat Anchor Bar Defect

    BMW is recalling 2015-2019 X6 and X6 M vehicles because rear seat lower anchor bars may damage when used with rigid child seat connectors, increasing injury risk in a crash.

    Product
    BMW — BMW X6, X6 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0281-2020·2019-11-13

    GE Healthcare Recalls Giraffe OmniBed Carestation CS1 Due to Fastener Risk

    GE Healthcare is recalling 59 Giraffe OmniBed Carestation CS1 devices because fasteners may be under-torqued, posing a risk that the canopy could detach and fall.

    Product
    Giraffe OmniBed Carestation CS1 - Product Usage: The device can be operated as an incubator or as a warmer and can transition from one mode to the other on user s demand. It cannot be operated in both modes at the same time. Incubators and warmers provide heat in a controlled man
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V800000·2019-11-06

    Mercedes-Benz Sprinter Recall for Front Seat Weld Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because a front seat weld may break in a crash, increasing injury risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V784000·2019-10-31

    Honda Recalls Pilot and Passport for Incomplete Body Welding

    Honda is recalling 2019-2020 Pilot and 2019 Passport vehicles because front frame members may not be fully welded, potentially reducing crash protection.

    Product
    HONDA — HONDA PILOT, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V778000·2019-10-30

    Temp-Air Recalls 2017-2019 EBB-80 Trailers Due to Hitch Coupling Defect

    Temp-Air is recalling 2017-2019 EBB-80 trailers because an incorrect hitch coupling may limit adjustability, potentially causing the trailer to drag and increasing crash risk.

    Product
    TEMP AIR — TEMP AIR EBB-80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0169-2020·2019-10-30

    OMNI Hip System Femoral Component Recalled for Missing Porous Coating

    OMNIlife science Inc. is recalling three OMNI Hip System femoral components because they are missing the required porous coating.

    Product
    OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral component of a primary or revision total hip replacement.
    Category
    Medical Device
    Distribution
    2 states