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.

701–725 of 2056

  • HighCPSC·18226·2018-09-21

    Woodcraft Recalls Motorcycle Handlebar Adapters Due to Crash Hazard

    Woodcraft is recalling clip-on adapter plates for Yamaha and Ducati motorcycles because they can crack and fail, posing a crash hazard. No injuries have been reported.

    Product
    Woodcraft clip-on adapters for motorcycle handlebars
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V643000·2018-09-19

    Livin' Lite CampLite Travel Trailers Recalled for Drawbar Crack Risk

    Livin' Lite is recalling 2017-2019 CampLite travel trailers because the drawbar may crack, causing the trailer to separate from the tow vehicle.

    Product
    LIVIN' LITE — LIVIN' LITE CAMPLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3024-2018·2018-09-19

    Intuitive Surgical Recalls da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors

    Intuitive Surgical is recalling 23,064 da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors because cracks in the extension tube may cause plastic fragments to fall into patients.

    Product
    da Vinci S/Si EndoWrist 8mm Monopolar Curved Scissors Model No. 420179-16 Product Usage: EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation of tissue, including: grasping, cutting, blunt and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-3025-2018·2018-09-19

    Intuitive Surgical Recalls da Vinci EndoWrist Scissors Due to Cracking Risk

    Intuitive Surgical is recalling 42,274 da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors because cracks may form in the extension tube, potentially causing fragments to fall into patients.

    Product
    da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. 470179-14 Product Usage: EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation of tissue, including: grasping, cutting, blunt and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V633000·2018-09-14

    Cruiser RV Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Cruiser RV is recalling 2019 travel trailers because missing inner bearing races may cause hub failure and increase crash risk.

    Product
    CRUISER RV — CRUISER RV RADIANCE ULTRA LITE, FUN FINDER EXTREME LITE, SHADOW CRUISER ULTRA LITE, MPG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V638000·2018-09-14

    Trail King Recalls 2016-2018 Trailers Due to Cracking Cross Members

    Trail King is recalling 2016-2018 ACS and AACS trailers because aluminum cross members may crack, potentially causing the suspension to loosen and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING AACS, ACS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V624000·2018-09-13

    Forest River Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Forest River is recalling 2019 travel trailers because missing inner bearing races may cause hub overheating or separation, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN XLR, VIBE, SIERRA, SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V616000·2018-09-12

    Highland Ridge RV Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Highland Ridge RV is recalling 2019 Open Range and Mesa Ridge travel trailers because missing inner bearing races may cause hub failure and increase crash risk.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE ULTRA LITE, OPEN RANGE LITE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2960-2018·2018-09-12

    Bayer Overhead Counterpoise Systems Recalled for Potential Structural Failure

    Bayer Medical Care is recalling two Overhead Counterpoise Systems because overtightened bolts may compromise structural integrity, posing a risk of injury.

    Product
    Overhead Counterpoise Systems (OCS), OCS CONF,STD CEIL MNT, STD HORZ ARM, Catalog # OCS 115A, Material Number 59880253
    Category
    Medical Device
    Distribution
    3 states
  • SevereNHTSA·18V617000·2018-09-12

    Altec Recalls 2018 Cranes, Derricks, and Aerial Devices Due to Fastener Defect

    Altec Industries is recalling 2018 cranes, digger derricks, and aerial devices because overtightened fasteners may break, potentially causing the platform to separate from the vehicle.

    Product
    ALTEC — ALTEC DIGGER DERRICK, CRANE, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2962-2018·2018-09-12

    Bayer Medical Care Recalls Overhead Counterpoise Systems Due to Structural Risk

    Bayer Medical Care is recalling four Overhead Counterpoise Systems because overtightened bolts may compromise structural integrity, posing a risk of injury.

    Product
    Overhead Counterpoise Systems (OCS), OCS, 580mm CEILING MOUNT, PORTEGRA2, Catalog # OCS CEIL 58, Material Number 84433765
    Category
    Medical Device
    Distribution
    3 states
  • SevereFDA (Devices)·Z-2961-2018·2018-09-12

    Bayer Overhead Counterpoise Systems Recalled for Potential Structural Failure

    Bayer Medical Care is recalling one Overhead Counterpoise System unit due to potential overtightening of bolts that could compromise structural integrity.

    Product
    Overhead Counterpoise Systems (OCS) OCS CONF an accessory device for use with Bayer injector systems as a support for an injector head. , SHORT CEIL MNT, STD HORZ ARM, Catalog # OCS 115AS, Material Number 59880288
    Category
    Medical Device
    Distribution
    3 states
  • HighCPSC·18219·2018-09-11

    Jimco Recalls Bistro Chairs Due to Seat Breakage and Fall Hazard

    Jimco is recalling about 16,000 outdoor folding bistro chairs because the seats can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a refund.

    Product
    Bistro chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V590000·2018-09-05

    Fabform Recalls 2017-2018 Power Tilt Dump Trailers Due to Hinge Fracture Risk

    Fabform is recalling 2017-2018 Power Tilt dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.

    Product
    FABFORM — FABFORM POWER TILT DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2937-2018·2018-09-05

    MedComp Duo-Flow XTP Straight Full Set Recalled for Suture Wing Cracking

    Medical Components, Inc. is recalling Duo-Flow XTP Straight Full Sets because suture wings may crack or break, posing risks of catheter dislocation, bleeding, and air emboli.

    Product
    Duo-Flow XTP Straight Full Set, RMS02105 RMS02108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18765·2018-09-05

    Polaris Recalls 2018 Ranger Recreational Off-Highway Vehicles Due to Crash Hazard

    Polaris is recalling about 1,000 model year 2018 Ranger 500, 570, EV, and EV LI-ION vehicles because front lower control arms can separate, posing a crash hazard.

    Product
    Model year 2018 Polaris Ranger 500, Ranger 570, Ranger EV, and Ranger EV LI-ION recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2934-2018·2018-09-05

    MedComp Recalls Duo-Flow Hemodialysis Catheter Sets Due to Suture Wing Cracking

    Medical Components, Inc dba MedComp is recalling Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Sets because suture wings may crack or break, posing a risk of patient injury.

    Product
    Duo-Flow Double Lumen Soft Tip CRRT/ABP Catheter Set; DL11/24 . Hemodialysis catheter insertion kits
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2753-2018·2018-08-29

    Handicare P600 Series Patient Lift Recalled for Strap Wear and Breakage

    Handicare USA Inc. is recalling four P600 Series patient lifts due to premature strap wear and breakage at maximum weight conditions.

    Product
    Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2752-2018·2018-08-29

    Handicare C Series Patient Lifts Recalled for Premature Strap Wear

    Handicare USA Inc. is recalling 716 C Series Patient Lifts because straps may wear and break prematurely at maximum weight conditions.

    Product
    Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V565000·2018-08-27

    Fabform Recalls 2018 EPT Dump Trailers Due to Hinge Fracture Risk

    Fabform is recalling 2018 EPT dump trailers because welded hinges may fracture, causing the dump box to fall unexpectedly and increasing the risk of injury or death.

    Product
    FABFORM — FABFORM DUMP TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2737-2018·2018-08-15

    Natus Neurology Recalls ErgoJust Video Carts Due to Pole Failure Risk

    Natus Neurology is recalling 797 ErgoJust mobile video carts because a manufacturing defect may cause the video pole to fail.

    Product
    Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video Extension, EuroJust ICU Cart Export For PTZ Video Ext. Video cart used for mobile medical record documentation.
    Category
    Medical Device
    Distribution
    47 states
  • HighFDA (Devices)·Z-2604-2018·2018-08-15

    New Era Orthopaedics Recalls Modera Pedicle Screw Shank Insertion Instrument

    New Era Orthopaedics is recalling 6 shank insertion instruments for the Modera Modular Pedicle Screw System due to a laser weld failure reported after excessive force was applied.

    Product
    Modera Modular Pedicle Screw System Shank Insertion Instrument, 3-107-07
    Category
    Medical Device
    Distribution
    2 states