The Recall Desk

Hazard

Mechanical Failure recalls

1,703 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,703
Critical
7
Severe
366
Most recent
2026-10-21

Of the 1,703 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.

401–425 of 1703

  • HighFDA (Devices)·Z-0804-2020·2020-01-22

    Flexicare BriteBlade Pro Laryngoscope Blades Recalled for Loose Components

    Flexicare Medical Ltd. is recalling BriteBlade Pro laryngoscope blades because internal components may become loose and separate, posing a risk of entering the patient's oral cavity.

    Product
    BriteBlade Pro Single-Use Fiber Optic Handle and Blade Miller 2, CE 0120, Do not Re-use, Rx Only, REF: 040-342U, Sterile EO, Qty 10, UDI: (01)15055788724053(17)230901(10)181002320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0781-2020·2020-01-15

    Stryker Pin To Rod Coupling Recalled for Clamping Failure

    Stryker is recalling Pin To Rod Couplings for the Hoffmann II Compact External Fixation System because they may fail to clamp the pin and rod as intended.

    Product
    Stryker Pin To Rod Coupling External Fixation System Hoffmann II Compact - Pin To Rod Coupling 5/3-4mm Catalog #: 4940-1-020 - Product Usage: Indications Distal radius fractures (intra and extra) articular Intercarpal fracture dislocations Unstable forearm fractures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0765-2020·2020-01-08

    Villa Sistemi Medicali Recalls Apollo DRF X-ray Tables Due to Chain Failure

    Villa Sistemi Medicali is recalling seven Apollo DRF X-ray tables because the angulation chain may fail early due to metal fatigue.

    Product
    Apollo DRF, Model Number 9784220831 - Product Usage: The remote controlled table Apollo DRF is an X-ray equipment that allows to perform general radiographic and fluoroscopic examinations. The system is a fixed position type. The movements of the table and tube support are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0766-2020·2020-01-08

    Villa Sistemi Medicali Recalls Apollo EZ X-Ray Table Due to Chain Failure

    Villa Sistemi Medicali is recalling one Apollo EZ X-ray table because the angulation chain may fail early due to metal fatigue.

    Product
    Apollo EZ, Model Number 9784152036 - Product Usage: The Apollo EZ remote-controlled table is X-ray equipment that can be used to perform general radiographic and fluoroscopic examinations. The system is a fixed position type. The movements of the table and tube support are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0772-2020·2020-01-08

    Nucletron Flexitron Brachytherapy Afterloader Recalled for Cable Guide Failure

    Nucletron BV is recalling 383 Flexitron brachytherapy afterloader systems due to a component failure that may cause treatment interruption or incorrect source positioning.

    Product
    There is a complaint regarding internal check cable guide mechanism failure for the Nucletron Flexitron brachytherapy afterloader system. Due to an obstruction during the check cable out drive, the internal guiding tube became displaced and the check cable became damaged. This…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0764-2020·2020-01-08

    Villa Sistemi Medicali Recalls Apollo X-ray Tables Due to Chain Failure Risk

    Villa Sistemi Medicali is recalling three Apollo X-ray tables because the angulation chain may fail early due to metal fatigue.

    Product
    Apollo, Model Numbers 9784100231, 9784120131, 9784130131 - Product Usage: Apollo table is a remote controlled X-ray system suitable for radiography and fluoroscopy examinations. The system is stationary mounted. The movements of the table and the tube stand are motorized and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0763-2020·2020-01-08

    Villa Sistemi Medicali Recalls Juno DRF X-Ray Systems Due to Chain Failure

    Villa Sistemi Medicali is recalling 46 Juno DRF x-ray systems because the angulation chain may fail early due to metal fatigue.

    Product
    Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0767-2020·2020-01-08

    Medtronic Recalls O-arm O2 Imaging Systems Due to Belt Loosening

    Medtronic is recalling 90 O-arm O2 Imaging Systems because a manufacturing issue may cause the gantry tractor motor drive belt to loosen, potentially rotating 3D images relative to the patient's physical position.

    Product
    O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Devices)·Z-0695-2020·2019-12-25

    Siemens Artis zee X-Ray System Recalled for Collision Sensor Defect

    Siemens is recalling three Artis zee Interventional Fluoroscopic X-Ray Systems because a collision sensor defect may block tabletop movement, potentially delaying or interrupting procedures.

    Product
    Artis zee/ zeego Interventional Fluoroscopic X-Ray System, Model Number: 10094142, Software Version: VC21C
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0707-2020·2019-12-25

    Medtronic Percutaneous Pin Adapter Recall for Potential Rotation

    Medtronic is recalling 1,297 percutaneous pin adapters because they may rotate after surgical placement and fail to return to their original position.

    Product
    Medtronic Adapter Percutaneous Pin, REF 9734752 (GTIN 00643169529489) and REF 9734752-G02 (GTIN 00763000054915), contained in the following kits: Upgrade Set Percutaneous Pin, REF 9735502 (GTIN 00643169529533) and REF 9735502-G02 (GTIN 00763000208462); Medtronic Adapter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0659-2020·2019-12-18

    Medtronic Biopsy Needle FPU Kit Recalled for Depth Stop Issue

    Medtronic Navigation is recalling Biopsy Needle FPU Kits because the depth stop may not tighten securely, potentially causing surgery delays.

    Product
    Biopsy Needle FPU Kit, Product # 9736075, UDI: 00763000063108
    Category
    Medical Device
    Distribution
    49 states
  • HighFDA (Devices)·Z-0586-2020·2019-12-11

    Steris Evolution Loading Car and Transfer Carriage Recall for Locking Pin Defect

    Steris Corporation is recalling 237 Evolution Loading Cars and Transfer Carriages because a locking pin defect may cause the equipment to fall forward unexpectedly.

    Product
    Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer, Steam
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V869000·2019-12-06

    Daimler Recalls 2020-2021 Thomas Built Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 145 school buses due to loose fan hub bolts that could damage components or detach, risking injury during an uncontrolled stop.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0517-2020·2019-12-04

    Zimmer Biomet Recalls 73 Calcar Trimmer Shafts for Mating Failure

    Zimmer Biomet is recalling 73 units of the ASI 2.0 Calcar Trimmer Shaft because the shaft end may fail to mate effectively with the broach.

    Product
    ASI 2.0 Calcar Trimmer Shaft for Use with Biomet¿ Rasp, Model Number 110032331
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·19E082000·2019-12-03

    Zamzow Aero Easy Cover tarping pawl assembly recall issued

    Zamzow is recalling one Aero Easy Cover tarping pawl assembly because a missing weld may cause the part to separate, increasing injury risk.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0496-2020·2019-11-27

    Teleflex Recalls WECK AutoEndo5 Clip Appliers Due to Jamming Risk

    Teleflex Medical is recalling WECK AutoEndo5 clip appliers because a component discrepancy may cause jamming or misloading, leading to clip failure during surgery.

    Product
    WECK AutoEndo5, Automatic Hem-O-Lok Clip Applier, REF AE05ML Automatic Endoscopic Surgical Ligating Clip Appliers are delivery devices for Hem-o-lok ML non-absorbable polymer ligating clips
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0353-2020·2019-11-20

    Heritage Medical 2000 Vascular Beds Recalled for Sudden Head Drop Hazard

    Heritage Medical Products is recalling 167 2000 Vascular beds due to a potential for the head of the bed to drop suddenly while a patient is lying on it.

    Product
    2000 Vascular with 30 Degree option
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V831000·2019-11-19

    Thomas Built Buses Recalling Saf-T-Liner HDX School Buses for Torque Converter Defect

    Daimler Trucks North America is recalling 2018-2020 Thomas Built Saf-T-Liner HDX school buses because loose torque converter fasteners may disable the vehicle, increasing injury risk during evacuation.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0172-2020·2019-11-13

    Medtech Rosa Brain 3.0 Neurosurgical Device Recalled for Trajectory Errors

    Medtech SAS is recalling 93 Rosa Brain 3.0 neurosurgical devices because the instrument holder may send tools on incorrect trajectories, potentially leading to improper device placement.

    Product
    Rosa Brain 3.0, Model No. ROSA 3.0. The device is delivered assembled in a wooden case and protected with plastic bubble and plastic film. Seals are put on the crate. The product is not shipped sterile. The device is intended for the spatial positioning and orientation of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0269-2020·2019-11-13

    Ortho-Clinical Diagnostics Recalls VITROS K+ Slides Due to Dispense Issues

    Ortho-Clinical Diagnostics is recalling VITROS K+ Slides because a mechanical failure may cause intermittent slide dispense issues.

    Product
    VITROS chemistry Products K+ Slides, Catalog No. 8157596. MicroSlides which contain reagents in a dry, multi-layered form.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0268-2020·2019-11-13

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Cl- Slides Due to Dispense Issues

    Ortho-Clinical Diagnostics is recalling VITROS chemistry Cl- Slides because the anti-backup platen may fail to advance, causing intermittent slide dispense issues.

    Product
    VITROS chemistry Products Cl- Slides, Catalog No. 8445207 (which does NOT support Urine CL-). MicroSlides which contain reagents in a dry, multi-layered form.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0270-2020·2019-11-13

    Pega Medical Recalls SCFE Knobs for Driver Due to Screw Loosening Risk

    Pega Medical Inc. is recalling 31 SCFE Knobs for Driver because screws may loosen during ultrasonic cleaning and fall out.

    Product
    SCFE (slipped capital femoral epiphysis) Knobs for Driver, 6.5mm and 7.3 mm Orthopedic surgical instrument component, for hip surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0286-2020·2019-11-13

    Biomedical Polymers Recalls Hemo-Drop Blood Dispensers Due to Metal Cannula Defect

    Biomedical Polymers, Inc. is recalling 108,000 Hemo-Drop Blood Dispensers because the metal cannula may break or fail to pierce the specimen tube.

    Product
    Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0267-2020·2019-11-13

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Cl- Slides for Dispense Issues

    Ortho-Clinical Diagnostics is recalling VITROS chemistry Cl- Slides because an anti-backup platen failure may cause intermittent slide dispense issues.

    Product
    VITROS chemistry Products Cl- Slides, Catalog No. 6844471 (which supports Urine CL-). MicroSlides which contain reagents in a dry, multi-layered form.
    Category
    Medical Device
    Distribution
    Distributed nationwide