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.

1326–1350 of 1694

  • HighFDA (Devices)·Z-0925-2014·2014-02-12

    CareFusion Recalls SmartSite Needleless Connectors Due to Connection Issues

    CareFusion is recalling SmartSite Needleless Connectors because they may unintentionally disconnect, be difficult to disconnect, or fail to disconnect from a female luer.

    Product
    SmartSite Needleless Connector, Model No. 2000E The SmartSite Needleless Connectors are sterile, individually packaged connectors. The connectors are used to administer fluid and medications. The needle free connector allows the user to add medication into the primary line wi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V072000·2014-02-12

    R&M Trailer Recalls 2012-2013 Enclosed Cargo Trailers Due to Door Lock Defect

    R&M Trailer is recalling 185 model year 2012-2013 enclosed cargo trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    R&M TRAILER — R&M TRAILER 6X12 ENCLOSED CARGO, 7X16 ENCLOSED CARGO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0926-2014·2014-02-12

    ArjoHuntleigh Rotoprone Therapy System Recalled for Lock Pin Malfunction

    ArjoHuntleigh is recalling 231 Rotoprone Therapy Systems because a lock pin can become stuck, preventing patients from being positioned prone.

    Product
    The Rotoprone therapy System is an advanced patient care system for the treatment and prevention of pulmonary complications. The Rotoprone Therapy System provides up to 62 degrees in both prone and supine positions as well as Trendelenburg/Reverse Trendelenburg positioning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V038000·2014-02-05

    Four Wheel & Six-Pac Truck Campers Recalled for Door Lock Defect

    Four Wheel & Six-Pac is recalling 2006-2013 truck campers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.

    Product
    FOUR WHEEL & SIX-PAC — FOUR WHEEL & SIX-PAC TRUCK CAMPERS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0828-2014·2014-02-05

    Accuray CyberKnife Robotic Radiosurgery System Recall for Mounting Assembly Issue

    Accuray is recalling 302 CyberKnife systems worldwide due to a potential safety issue where the Synchrony Boom Arm Mounting Assembly may detach.

    Product
    Accuray CyberKnife Robotic Radiosurgery System; Accuray Incorporated Sunnyvale, CA. Indicated for treatment planning and image guided stereotactic radiosurgery and precision radiotherapy.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0857-2014·2014-02-05

    Sorin CP5 Centrifugal Pump System Recalled for Control Knob Failures

    Sorin Group is recalling 75 CP5 centrifugal pump systems due to reports of pump speed control knob failures that result in no response.

    Product
    CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0855-2014·2014-02-05

    Orthofix Firebird Modular Screw Driver Recalled for Collet Malfunction

    Orthofix is recalling 443 Modular Screw Drivers because the collet may malfunction, preventing effective screw placement and delaying surgery.

    Product
    Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw Driver, Product Usage: The Modular Screw Driver is used for inserting a modular bone screw into the pedicle during a spinal fixation procedure. It is a reusable instrument.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V039000·2014-02-05

    Nomad Recalls 2013 Dispatch Trailers Due to Door Lock Jamming Risk

    Nomad is recalling 2013 Dispatch 14A, 20SS0, and 16AS0 trailers because a door lock defect could jam the deadbolt, trapping occupants inside.

    Product
    NOMAD — NOMAD DISPATCH 20SS0, DISPATCH 14A, DISPATCH 16AS0
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0856-2014·2014-02-05

    Sorin S5/C5 Heart-Lung Machine Recalled for Pump Control Failures

    Sorin Group is recalling S5/C5 Heart-lung machines and CP5 centrifugal pump systems due to pump speed control knob failures that result in no response.

    Product
    S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0825-2014·2014-02-05

    Siemens ACUSON SC2000 Ultrasound System Recalled for Control Panel Lock Failure

    Siemens is recalling 271 ACUSON SC2000 ultrasound systems because the control panel locking mechanism can fail, making the device difficult to steer during transport.

    Product
    ACUSON SC2000 Power Input: 100-240VAC, 1600 Max 50/60Hz; Siemens Medical Solutions USA, Inc. 685 East Middlefield Road Mountain View, CA 94043 Ultrasound imaging system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0786-2014·2014-01-29

    Siemens Recalls SimView NT Radiation Therapy Simulation Systems

    Siemens is recalling 65 SimView NT radiation therapy simulation systems worldwide because a rare mechanical failure could prevent the stopping of intended component movements.

    Product
    SIMVIEW NT and SIMVIEW NT with IDI: October 01, 2012 Siemens ceased Simview distribution. Manufactured by: Mecaserto now known as Mecasim Parc de lEsplanade 9,Rue Niels Bohr 77400 Saint Thibault des Vignes- France The intended use of the SIEMENS branded SIMVIEW NT
    Category
    Medical Device
    Distribution
    7 states
  • HighNHTSA·14V017000·2014-01-27

    Nu Wa Recalls 2011-2013 Hitchhiker Trailers Due to Door Lock Defect

    Nu Wa Industries is recalling 2011-2013 Hitchhiker fifth wheel trailers because a door lock defect may jam the deadbolt, trapping occupants inside.

    Product
    HITCHHIKER — HITCHHIKER LS, DISCOVER AMERICA, CHAMPAGNE EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0747-2014·2014-01-22

    GE Healthcare Carescape Patient Data Module Recall for Latch Failure

    GE Healthcare is recalling Carescape Patient Data Modules due to a potential safety issue involving the intermittent failure of the spring-loaded mounting latch.

    Product
    GE Healthcare Carescape Patient Data Module The Patient Data Module (PDM) is intended to provide uninterrupted acquisition of physiologic parameter data on adult, pediatric and neonatal patients during non-transport/bedside and transport patient care episodes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V003000·2014-01-17

    EverGreen Recalls 2013 Travel Trailers Due to Door Lock Jamming Risk

    EverGreen is recalling 2013 travel trailers because a door lock defect could jam the deadbolt, trapping occupants inside the vehicle.

    Product
    EVERGREEN — EVERGREEN EVER-LITE SELECT, ASCEND, I-GO, EVER-LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0654-2014·2014-01-15

    Anspach Pneumatic Drill System Recalled Due to Hose Rupture Risk

    The Anspach Effort, Inc. is voluntarily removing Pneumatic Drill Systems from the market because the outer hose on the motor hand-piece can rupture without warning if air flow is blocked.

    Product
    ***REF BLACKMAX-N***Swivel/Angle Motor Assembly***Rx Only***The Anspach Effort, Inc. Intended for cutting and shaping bone.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0651-2014·2014-01-15

    Midmark Vantage Panoramic X-Ray System Recalled for Firmware Error

    Midmark Corp dba Progeny Inc is recalling 58 Vantage Panoramic X-Ray systems due to a firmware error that may cause the unit's column to continue moving vertically after the control button is released.

    Product
    The Vantage Digital Panoramic System delivers high-value features standard on every system: - Five pre-programmed exam settings, including bitewing, minimize exam set-up time and allow routine diagnostic exams to be performed extraorally for improved clinical efficiency and patie
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0647-2014·2014-01-15

    On Site Gas Systems POGS 33C Portable Oxygen System Recall

    On Site Gas Systems is recalling 198 POGS 33C portable oxygen generation systems in Pennsylvania because the heat exchanger hose may fail.

    Product
    On Site Gas Systems POGS 33C Portable Oxygen Generation System
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Devices)·Z-0618-2014·2014-01-08

    Stryker S3 Med/Surg Bed Recall for Foot End Cover Damage

    Stryker is recalling S3 Med/Surg beds due to potential damage to the Foot End Cover and Power Coil Cable caused by reduced clearance.

    Product
    S3 Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals. The bed is designed for a 15 year expected service life under normal use conditions, and with appropriate periodic maintenance as described in the maintenance manual
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0617-2014·2014-01-08

    Stryker Secure II Med/Surg Beds Recalled for Potential Cover Damage

    Stryker is recalling Secure II and S3 Med/Surg beds due to potential damage to the Foot End Cover and Power Coil Cable caused by reduced clearance.

    Product
    Secure II Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals. The bed is designed for a 15 year expected service life under normal use conditions, and with appropriate periodic maintenance as described in the maintenance
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0616-2014·2014-01-08

    Steris SYSTEM 1E Liquid Chemical Sterilant Processing System Recalled for Valve Issues

    Steris Corporation is recalling SYSTEM 1E Liquid Chemical Sterilant Processing Systems because check valve o-rings degrade, causing nuisance aborts.

    Product
    SYSTEM 1E Liquid Chemical Sterilant Processing System, Distributed by STERIS Corporation, Mentor, OH The SYSTEM 1E Liquid Chemical Sterilant Processing System is intended for the liquid chemical sterilization of manually cleaned immersible and reusable critical and semi-critic
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0581-2014·2014-01-01

    Smith & Nephew Recalls Reflection Acetabular Liners Due to Tolerance Issues

    Smith & Nephew is recalling 38 units of Reflection acetabular liners because they may be out of tolerance and fail to fully seat into the shell.

    Product
    REFLECTION(R), MICROSTABLE(R), ACETABULAR LINER, 20o OVERHANG, 28 MM ID, 54-56 OD, QTY: (1), STERILE EO, REF 71742854, Smith & Nephew, Inc. Memphis, TN 38116 USA. Orthopaedic.
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·13V647000·2013-12-26

    Bay Bridge Manufacturing Recalls Cargo Vans and Trailers with Jamming Door Locks

    Bay Bridge Manufacturing is recalling 2006-2013 cargo vans and trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.

    Product
    BAY BRIDGE MFG — BAY BRIDGE MFG FRP UNIT, CLASSIC UNIT, SHEET AND POST UNIT, SHEET & POST UNIT TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0533-2014·2013-12-25

    Integra Epidural Anesthesia Kits Recalled Due to Syringe Plunger Defect

    Integra LifeSciences is recalling specific lots of epidural anesthesia kits because the included BD LOR syringe plunger may stall or stick.

    Product
    Integra Disposable, Convenience Kit Single Shot Epidural Tray Reorder Number 340269 Rx Only Product Usage: The Integra kits which contain a BD LOR syringe are intended to provide licensed medical professionals with a kit containing drugs and other medical devices that are u
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0521-2014·2013-12-25

    Intuitive Surgical Recalls Large Needle Drivers Due to Jaw Insert Detachment Risk

    Intuitive Surgical is recalling Large Needle Drivers for the da Vinci S and Si systems because the jaw insert may detach during use.

    Product
    Large Needle Driver, 8MM assembly of the da Vinci S IS1200 and da Vinci Si, IS2000. Manufactured by Intuitive Surgical, Sunnyvale, CA. EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation
    Category
    Medical Device
    Distribution
    Distributed nationwide