The Recall Desk

Hazard

Mechanical Failure recalls

1,704 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,704
Critical
7
Severe
366
Most recent
2026-10-22

Of the 1,704 mechanical failure recalls we have scored against our rubric, 7 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 366 (21%) 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 mechanical 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 1704

  • HighFDA (Devices)·Z-3165-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 13 mm x 300 mm, Item Number: 814613300
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3158-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 380 mm, Item Number: 814611380
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3152-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 9 mm x 460 mm, Item Number: 814609460
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3159-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 130¿ 11 mm x 400 mm, Item Number: 814611400
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3067-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 125¿ 13 mm x 260 mm, Item Number: 814313260
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3108-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail 130¿ 9 mm x 180 mm, Item Number: 814509180
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3112-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Set Screw Defect

    Zimmer Biomet is recalling 5,947 Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Right 130¿ 9 mm x 320 mm, Item Number: 814509320
    Category
    Medical Device
    Distribution
    42 states
  • HighFDA (Devices)·Z-3105-2018·2018-09-19

    Zimmer Biomet Recalls Affixus Hip Fracture Nail Due to Set Screw Defect

    Zimmer Biomet is recalling Affixus Hip Fracture Nails because the set screw cannot advance or reverse from its original position.

    Product
    Affixus¿ Hip Fracture Nail Left 125¿ 13 mm x 400 mm, Item Number: 814413400
    Category
    Medical Device
    Distribution
    42 states
  • HighNHTSA·18V640000·2018-09-18

    Forest River Recalls Buses with Defective Wheelchair Lifts

    Forest River is recalling specific 2012-2018 buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, ELKHART, GLAVAL BUS ALLSTAR XL MVP, ALLSTAR, SENATOR II, STARLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V611000·2018-09-11

    Coach and Equipment Transit Buses Recalled for Wheelchair Lift Defect

    Coach and Equipment is recalling certain transit buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, METRO LITE, CONDOR LT, PEGASUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V603000·2018-09-10

    Turtle Top Transit Buses Recalled for Wheelchair Lift Cam Failure

    Turtle Top is recalling 2013-2018 Odyssey, VanTerra, and Terra Transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high.

    Product
    TURTLE TOP — TURTLE TOP VANTERRA, ODYSSEY, TERRA TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2878-2018·2018-09-05

    Biosense Webster Recalls WaveCrest Left Atrial Appendage Occlusion System Devices

    Biosense Webster is recalling 25 units of the WaveCrest Left Atrial Appendage Occlusion System (32 mm) because the delivery sheath may buckle during recapture.

    Product
    WaveCrest Left Atrial Appendage (LAA), Occlusion System (32 mm), Catalog Numbers WCR1523 and WCR2523.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2955-2018·2018-09-05

    GE Carestation 30 Anesthesia Systems Recalled for Gas Switch Defect

    GE Medical Systems is recalling 252 Carestation 30 anesthesia systems worldwide because a gas switch may unexpectedly change position, potentially causing hypoxia.

    Product
    GE Carestation 30 anesthesia systems
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2954-2018·2018-09-05

    GE Carestation Anesthesia Systems Recalled for Gas Switch Defect

    GE Medical Systems is recalling 310 anesthesia systems worldwide because a gas switch may unexpectedly change position, potentially causing hypoxia.

    Product
    GE Carestation 620/650/650c, A1 and A2 (non-US distribution) anesthesia systems
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2956-2018·2018-09-05

    GE 9100c NXT anesthesia systems recalled for gas switch defect

    GE Medical Systems is recalling 401 anesthesia systems worldwide because a gas switch may unexpectedly change position, potentially causing hypoxia.

    Product
    GE 9100c NXT anesthesia systems
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·18V584000·2018-09-04

    Collins School Bus Recall for Wheelchair Lift Cam Failure

    Collins Bus is recalling 2012-2018 school buses with Ricon wheelchair lifts because a cam may fail, causing the platform to rise too high and increasing injury risk.

    Product
    COLLINS — COLLINS SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V574000·2018-08-30

    Micro Bird School Bus Wheelchair Lift Cam Recall

    Micro Bird is recalling 2012-2018 school buses with specific wheelchair lifts because a cam may fail, allowing the platform to rise too high and increase injury risk.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, G5 SCHOOL BUS, MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V573000·2018-08-30

    Champion Recalls Buses with Defective Wheelchair Lifts

    Champion is recalling 2012-2018 buses with specific wheelchair lifts where a cam may fail, allowing the platform to rise too high and risk injury.

    Product
    CHAMPION — CHAMPION DEFENDER, AMERICAN CRUSADER, AMERICAN COACH, CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2837-2018·2018-08-29

    Siemens 3D TOP Ceiling Stand Recalled for Potential Rope Failure

    Siemens Medical Solutions is recalling 699 3D TOP Ceiling Stands because a load-bearing rope could break, causing the arm to drop and potentially seriously injure patients or users.

    Product
    3D TOP Ceiling Stand, model no. 3070039 3074486 3070013 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the detector and is moveable on a ceiling rail system in three axis. The tube and / or detector can be rotated above a horizontal and a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2838-2018·2018-08-29

    Siemens 3D V Ceiling Stand Recalled for Potential Rope Failure

    Siemens is recalling 3D V ceiling stands because the primary load-bearing rope could break, causing the arm to drop and potentially seriously injuring patients or users.

    Product
    3D V, model. no. 7042042 7042059 3070021 Product Usage: The ceiling stand is used to hold the X-ray tube and / or the detector and is moveable on a ceiling rail system in three axis. The tube and / or detector can be rotated above a horizontal and a vertical axle. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V563000·2018-08-24

    Navistar Recalls 2015-2019 IC Bus School Buses Due to Wheelchair Lift Defect

    Navistar is recalling 2015-2019 IC Bus school buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    IC BUS — IC BUS CESB, CASB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V560000·2018-08-23

    Thomas Built Buses Recalling Wheelchair Lifts Due to Cam Failure

    Daimler Trucks is recalling 2015-2019 Thomas Built Buses equipped with specific wheelchair lifts because a component may fail, allowing the platform to rise too high.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2661-2018·2018-08-15

    Arjohuntleigh Q-Connect Scale Recall Due to Spreader Bar Detachment Risk

    Arjohuntleigh Magog is recalling Q-Connect 272 KG Scales used with Maxi Sky 2 ceiling lifts because the spreader bar can detach from the scale attachment.

    Product
    Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling lift The Scale is intended to be used with patient lifters to measure the weight of a patient who cannot stand on a scale. It is designed to be used indoors in hospitals, nursing homes, home care or health care facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide