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.

1476–1500 of 2094

  • SevereNHTSA·15V884000·2015-12-29

    Micro Bird Recalls Transit Buses Due to Loose Wheel Bolt

    Micro Bird is recalling 2014-2016 G5 and MB II transit buses because a wheel bolt may be insufficiently torqued, posing a risk of vehicle misalignment and loss of control.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V880000·2015-12-28

    Tiffin Motorhomes Recall 2007-2015 Models Due to Unstable Entry Steps

    Tiffin is recalling 2007-2015 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    TIFFIN — TIFFIN BUS, ALLEGRO, ALLEGRO BAY, BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V876000·2015-12-23

    GM Recalls 2015 Chevrolet Cruze for Loose Seat Belt Bolts

    General Motors is recalling 2015 Chevrolet Cruze vehicles because a driver-side seat belt bolt may be loose. This defect could prevent the seat belt from holding in a crash.

    Product
    CHEVROLET — CHEVROLET CRUZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V877000·2015-12-23

    Entegra Motorhomes Recalled for Unstable Electric Entry Steps

    Entegra is recalling specific 2008-2011 motorhomes because a bolt on the electric steps may fracture, causing the steps to become unstable and increasing the risk of injury.

    Product
    ENTEGRA — ENTEGRA INSIGNIA, ASPIRE, CORNERSTONE, EMBLEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V872000·2015-12-23

    Holiday Rambler and Monaco Motorhomes Recalled for Unstable Entry Steps

    Allied Recreation Group is recalling specific Holiday Rambler and Monaco motorhomes because a bolt on the electric entry steps may fracture, causing instability and injury risk.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, MONACO, MONACO RV AMBASSADOR, ENDEAVOR, KNIGHT, NEPTUNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0420-2016·2015-12-23

    Verathon GlideScope Video Laryngoscope Blades Recalled for Potential Separation

    Verathon is recalling GlideScope Video Laryngoscope blades because silicone adhesive may fail, causing the blade halves to separate during use.

    Product
    GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4 - 0574-0001; GVL 5- 0574-0030. The system consists of a video laryngoscope and portable video monitor. The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0415-2016·2015-12-23

    MOOG Medical Devices Recalls EnteraLite Infinity Enteral Pump Delivery Sets

    MOOG Medical Devices Group is recalling EnteraLite Infinity Enteral Pump Delivery Sets because the purple ENFit connector may crack or break, causing leaks.

    Product
    Catalog No. INF0020-A  EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Connector (spiked set); Catalog No. INF0500-A - 500ml EnteraLite Infinity Enteral Pump Delivery Set with ENFit Connector System and Transitional Stepped Conn
    Category
    Medical Device
    Distribution
    1 state
  • SevereNHTSA·15V862000·2015-12-22

    MCI Recalls 2016 J4500 Motor Coaches Due to Seat Mounting Defect

    Motor Coach Industries is recalling 2016 MCI J4500 motor coaches because a seat mounting bolt may be installed incorrectly, increasing injury risk in a crash.

    Product
    MCI — MCI J4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V837000·2015-12-14

    MCI Recalls 2015 Motor Coaches Due to Missing Axle Welds

    Motor Coach Industries is recalling specific 2015 D4500 and D4505 motor coaches because drive axles may be missing welds on hanger brackets, which could separate and affect vehicle control.

    Product
    MCI — MCI D4500, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V833000·2015-12-11

    GM Recalls 2016 Acadia, Traverse, Enclave for Seat Frame Weld Defect

    General Motors is recalling 2,633 model year 2016 Chevrolet Traverse, GMC Acadia, and Buick Enclave vehicles because the third-row left lower seat frame may have welds in incorrect locations.

    Product
    GMC — GMC, CHEVROLET, BUICK ACADIA, TRAVERSE, ENCLAVE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0349-2016·2015-12-09

    Philips INTEGRIS Vascular System Recall for Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling three INTEGRIS vascular systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare INTEGRIS vascular System Model : 722122 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0351-2016·2015-12-09

    Philips Allura Xper Cardio Systems Recalled for Ceiling Suspension Fall Risk

    Philips Medical Systems is recalling 16 Allura Xper cardio systems because the monitor ceiling suspension system may fall.

    Product
    Philips Healthcare Xper cardio systems Model : 722123 Product Usage: The Allura Xper series is intended for use in cardiovascular and vascular X-ray imaging applications including diagnostics, interventional procedures (such as PTCA, stent placement, embolization and throm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0356-2016·2015-12-09

    Baylis ProTrack Microcatheter Recalled for Circumferential Shaft Cracks

    Baylis Medical Corp is recalling 433 ProTrack Microcatheters nationwide due to circumferential cracks along the shaft.

    Product
    ProTrack Microcatheter. Model/Catalog Numbers CIC38-145, CIC35-145. Sterile, single use device intended to be used as a standard infusion wire or as an exchange guide for exchanging guidewires. Coaxial Injectable catheter guide wire. Cardiovascular.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V810000·2015-12-01

    Altec Recalls 2011-2015 Brush Chippers Due to Weld Defects

    Altec is recalling 2011-2015 DSC6 and DC610 brush chippers because improper welds or incorrect spacers may cause the anvil to detach, posing an injury risk.

    Product
    ALTEC — ALTEC DC610 BRUSH CHIPPER, DSC6 BRUSH CHIPPER
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V781000·2015-11-23

    Strick Dry Freight Van Trailer Recall for Rear Impact Guard Defect

    Strick Trailers is recalling 1998-2005 Dry Freight Van Trailers because rear impact guards may fail to prevent vehicles from sliding underneath during a crash.

    Product
    STRICK — STRICK DRY FREIGHT VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0246-2016·2015-11-18

    Teleflex Medical Recalls Rusch Flexi-slip Tracheal Tube Stylets

    Teleflex Medical is recalling Rusch Flexi-slip tracheal tube stylets because the plastic coating may split or break off.

    Product
    Rusch Flexi-slip tracheal tube Stylet, Size Ch 6, Sterile, Teleflex Medical.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15E088000·2015-10-28

    Recaro Commercial Bus Driver Seats Recalled for Missing Welds

    Johnson Controls is recalling Recaro Ergo-M Commercial Bus Driver Seats because missing welds may allow the seat belt anchorage to separate, increasing injury risk in a crash.

    Product
    SEATS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V697000·2015-10-23

    Honda Recalls 2015-2016 Fit Vehicles Due to Airbag Puncture Risk

    Honda is recalling 25,367 2015-2016 Fit LX vehicles because defective rear grab handle brackets may puncture side curtain airbags, increasing injury risk in a crash.

    Product
    HONDA — HONDA FIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V649000·2015-10-13

    Great Dane Recalls 2016 Trailers Due to Axle Nut Retaining Clip Defect

    Great Dane is recalling 2016 Dry Freight and Converter Dolly trailers because axle nut retaining clips may be missing or improperly seated, risking wheel loss and loss of vehicle control.

    Product
    GREAT DANE — GREAT DANE CONVERTER DOLLY, DRY FREIGHT SEMI-TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide