The Recall Desk

Hazard

Mechanical Failure recalls

1,694 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,694
Critical
7
Severe
304
Most recent
2026-09-02

Of the 1,694 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 304 (18%) 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.

1401–1425 of 1694

  • HighFDA (Devices)·Z-0284-2014·2013-11-20

    Hospira Recalls Plum A+ Infusion Systems Due to Broken Pressure Sensor Pin

    Hospira is recalling 10,669 Plum A+ Infusion Systems because the distal pressure sensor pin may break. This defect can prevent the device from detecting occlusions in the administration set.

    Product
    The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines in and one line out and can be used for standard, piggyback, or concurrent delivery. The Plum A+ Infusion System is designed to deliver parenteral, enteral, or epidural infusions o
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0210-2014·2013-11-20

    Integra LifeSciences Recalls Mayfield Skull Clamps Due to Locking Issues

    Integra LifeSciences is recalling 37 Mayfield Skull Clamps because the locking knob may not unlock easily or the torque knob may malfunction.

    Product
    Composite Series Skull Clamp, one clamp per tote. The MAYFIELD¿ Skull Clamp (A3059) is a cranial stabilization device, designed to provide rigid skeletal fixation. The Skull Clamp is placed on the patient's skull to hold their head and neck securely in a particular position w
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·13V575000·2013-11-19

    Space Craft Recalls Fifth Wheel Trailers Due to Door Lock Defect

    Space Craft is recalling 2006-2013 fifth wheel and travel trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    SPACE CRAFT — SPACE CRAFT FIFTH WHEEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0149-2014·2013-11-13

    Ethicon Endo-Surgery Recalls Adjustable Gastric Bands Due to Locking Failure

    Ethicon Endo-Surgery Inc is recalling adjustable gastric bands because they failed to meet force-to-lock requirements during aging studies.

    Product
    Adjustable Gastric Band, packaged alone in transparent PETG inner and outer blisters with Tyvek lids, or in various kit configurations with one band per kit. Product Usage: Intended for use in surgical treatment of morbid obesity
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0147-2014·2013-11-13

    Beckman Coulter Recalls UniCel DxH 800 and DxH 600 Hematology Analyzers

    Beckman Coulter is recalling 1,025 UniCel DxH 800 and DxH 600 hematology analyzers because specific check valves may fail, potentially causing air or liquid leaks.

    Product
    UniCel DxH 800 and DxH 600 Coulter Cellular Analysis Systems The UniCel DxH 800/DxH 600 analyzers are quantitative, multiparameter, automated hematology analyzers for in vitro diagnostic use in screening patient populations found in clinical laboratories. The DxH 800 is availa
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V565000·2013-11-13

    Sutphen Fire Apparatus Recall for Ladder Bearing Defect

    Sutphen is recalling specific fire apparatus models because ladder extension bearings may seize, causing cables to fail and the aerial to retract unexpectedly.

    Product
    SUTPHEN — SUTPHEN SPH 100, SP 110, SPI 112, SAI 110
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0167-2014·2013-11-13

    Invacare Aquatec Ocean Mobile Shower and Toilet Commode Recall

    Invacare is recalling Aquatec Ocean mobile shower and toilet commodes because backrest cushion fixtures may unlatch in reclined or tilted positions.

    Product
    Aquatec Ocean VIP, Aquatec Ocean Dual-VIP, Aquatec Ocean E-VIP mobile shower and toilet commode with tilting function. Mobile shower and toilet commode with tilting function
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0141-2014·2013-11-13

    Steris Harmony Equipment Management System Recalled for Drive Screw Failure Risk

    Steris Corporation is recalling 127 Harmony Equipment Management Systems because a drive screw in the ceiling supply unit may break, causing the adjustable arm to drop.

    Product
    Harmony Equipment Management System, Model #603X/80XX, STERIS Corporation, Mentor, OH Harmony Equipment Management Systems (EMS) are used in hospital facilities to provide ready access to medical gasses, electrical power and audio/visual data services, in addition to managing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0153-2014·2013-11-13

    Beckman Coulter ISE REF Valve Recall for Chemistry Analyzers

    Beckman Coulter is recalling ISE REF Valves for AU480, AU680, and AU5800 analyzers due to premature valve failure that may affect test accuracy.

    Product
    ISE REF Valve, Part No. MU7638 for the AU480, AU680, and AU5800 Chemistry Analyzer. Automated chemistry analyzers that measures analytes in samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13E067000·2013-11-07

    Lippert Travel Trailer Doors Recalled for Deadbolt Jamming Risk

    Lippert is recalling 2006-2013 travel trailer doors with Fastec deadbolts that may jam, potentially trapping occupants inside the vehicle.

    Product
    LATCHES/LOCKS/LINKAGES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0041-2014·2013-11-06

    Xoran MiniCAT CT Scanner Recalled for Gantry Rotation Failure

    Xoran Technologies is recalling 320 MiniCAT CT Scanners because the gantry may fail to rotate while emitting radiation.

    Product
    Xoran MiniCAT CT Scanner ID ENT00001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0089-2014·2013-11-06

    Philips Recalls BrightView XCT Gamma Cameras Due to Latch Failure

    Philips is recalling 371 BrightView XCT gamma cameras because the Flat Panel Detector may not remain securely latched in the stowed position.

    Product
    BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT), one unit per box. BrightView XCT is a gamma camera for Single Photon Emission Computed Tomography (SPECT) and integrates with an attenuation device consisting of flat panel x-ray imaging com
    Category
    Medical Device
    Distribution
    32 states
  • HighNHTSA·13V553000·2013-11-05

    Elite Cargo Trailer Recall for Door Lock Jamming Hazard

    Elite is recalling 2006-2013 cargo trailers with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    ELITE — ELITE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0060-2014·2013-10-30

    Integra Licox Brain Tissue Oxygen Monitoring Kit Recall for Hex Wrench Defect

    Integra LifeSciences is recalling Licox Brain Tissue Oxygen Monitoring Kits because a hex wrench may fail to loosen the set screw on the drill bit.

    Product
    Integra Licox Brain Tissue Oxygen Monitoring 1 x Dual Lumen Introducer Kit REF IM2_EU Rx Only, Manufacturer GMS- Gesellschaft fur medizinische, Sondentechnik mbH Dofstrasse 2 24247 Melkendorf, Germany Distributed by Integra Neurosciences 311 Enterprise Drive Plainsboro, N
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0033-2014·2013-10-30

    Philips MRI Systems Recalled for Potential Water Freezing in Venting System

    Philips Medical Systems is recalling 511 MRI systems because water may collect and freeze in the vent pipe, potentially blocking the magnet venting system.

    Product
    Philips MR Systems: Asset 0.5T, Apollo 0.5T, Infinion 1.5T, Eclipse/Polaris 1.5T, Panorama 0.6T 1.0T, Magnetic Resonance Imaging Systems intended for clinical/radiologic diagnostic imaging applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0012-2014·2013-10-23

    GE Healthcare X-ray Systems Recalled for Loose Power Assist Handle Bolts

    GE Healthcare is recalling 810 X-ray systems because internal bolts on the power assist handle may loosen or fall out, potentially causing the handle to stick in the ON position.

    Product
    GE Healthcare, Precision 500D, Legacy, RFX, and SFX X. This table is intended for use in a diagnostic X-ray system to support patients during general purpose radiological procedures in the horizontal, vertical and trendelenburg positions. - The Expedio 500D is designed to per
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V499000·2013-10-23

    Neo Trailers Recalls 2010-2011 Models Due to Door Lock Jamming Risk

    Neo Manufacturing is recalling 2010-2011 cargo trailers because a defect in Fastec door locks may jam the deadbolt, potentially trapping occupants inside.

    Product
    NEO TRAILERS — NEO TRAILERS NCV, NAS, NAV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V533000·2013-10-23

    Trailex Recalls Enclosed Car Trailers Due to Door Lock Jamming Risk

    Trailex is recalling certain enclosed car trailers because a defect in the door locks may jam the deadbolt, potentially trapping occupants inside.

    Product
    TRAILEX — TRAILEX CTE-80180, CTE-80210 HD, CTE-84180
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V522000·2013-10-18

    RC and MTI Enclosed Trailers Recalled for Door Lock Defect

    RC Trailers is recalling 2006-2013 RC and MTI enclosed trailers because a door lock defect could jam the deadbolt, trapping occupants inside.

    Product
    RC — RC, MTI ENCLOSED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E057000·2013-10-17

    Keyline Sales Recalls Exterior Doors for Potential Lock Jamming Hazard

    Keyline Sales is recalling exterior doors for cargo and specialty trailers built with Fastec-brand locks. The defect may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V479000·2013-10-17

    Shadow Trailers Recalls Horse Trailers Due to Door Lock Jamming Risk

    Shadow Trailers is recalling 2006-2012 gooseneck and bumperpull horse trailers because a defect in certain door locks may jam the deadbolt, potentially trapping occupants inside.

    Product
    SHADOW — SHADOW BUMPERPULL, GOOSENECK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V482000·2013-10-17

    Vintage Trailers Recall 2007-2013 Models Due to Door Lock Jamming Risk

    Vintage Trailers is recalling 4,212 travel trailers from 2007-2013 because a door lock defect could jam the deadbolt, trapping occupants inside the vehicle.

    Product
    VINTAGE — VINTAGE CARGO, OUTLAW, CRYSTAL, BANDIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V490000·2013-10-17

    KZRV Travel Trailer Recall for Door Lock Jamming Hazard

    KZRV is recalling 2006-2013 travel trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    KZRV — KZRV TOWABLE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V510000·2013-10-17

    Northwood Recalls Trailers With Defective Door Locks That May Jam

    Northwood is recalling specific travel trailers and campers because a defect in the door locks may jam the deadbolt, potentially trapping occupants inside.

    Product
    WOLF CREEK — WOLF CREEK, FOX MOUNTAIN, ARCTIC FOX PICKUP CAMPER, FIFTH WHEEL, TOY HAULER, TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2292-2013·2013-10-09

    Ebi Solitaire-35 Spinal Fusion Device Recalled for Screw Complaints

    Ebi, LLC is recalling 1,730 units of the Solitaire-35 PEAK Solitaire Anterior Spinal System due to complaints regarding one of the three screws driving through the cage.

    Product
    Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral body fusion device.
    Category
    Medical Device
    Distribution
    Distributed nationwide