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.

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 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.

1226–1250 of 1694

HighFDA (Devices)·Z-0209-2015·2014-11-19
American Medical Systems Recalls AMS 700 Series Inflatable Penile Prosthesis Accessory Kits
American Medical Systems is recalling AMS 700 Series Accessory Kits because supplier-supplied Keith needles may bend or break when used with the Furlow tool.
Product
AMS 700 Series Inflatable Penile Prosthesis Accessory Kit (AMS 700 Line Accessory Kit), 72401850. Keith Needles are part of the AMS 700 Accessory Kit. In conjunction with the Furlow Insertion Tool (Furlow), the Keith Needles facilitate the passing of the pulling sutures throug
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V727000·2014-11-12
Hino Recalls 2012-2015 XFC Vehicles Due to Hybrid Motor Shaft Defect
Hino is recalling 2012-2015 XFC vehicles because the hybrid motor output shaft may break, potentially causing the vehicle to stop moving and increasing crash risk.
Product
HINO — HINO XFC
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15022·2014-11-12
Aqua Lung Recalls Buoyancy Compensators Due to Drowning Hazard
Aqua Lung is recalling buoyancy compensators with SureLock II handles that may detach, posing a drowning risk. Consumers should stop using them and return them for free replacement.
Product
Aqua Lung buoyancy compensators with SureLock II weight pocket handles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0133-2015·2014-11-05
SAM Medical Products Recalls Junctional Tourniquet Auxiliary Straps
Sam Medical Products is recalling SJT 102 and 112 auxiliary straps because the snap hook broke during a training demonstration.
Product
SAM Junctional Tourniquet (SJT) Auxiliary, Model SJT 102 and SJT 112. The SJT models specific intended uses are to control difficult bleeds in the inguinal area and to immobilize a pelvic fracture.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0151-2015·2014-11-05
Joerns EasyCare Bed Recalled Due to Care-Lock Feature Failure Risk
Joerns Healthcare is recalling 3,135 EasyCare Beds because the Care-Lock feature may fail to stay engaged, posing a safety risk to patients.
Product
Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed is a device intended for medical purposes. The bed includes a built-in electric motor and remote controls that can be operated by the patient to adjust the height and surface contour of the bed.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0137-2015·2014-11-05
Animas Vibe Insulin Infusion Pump Recalled for Keypad Wear Issues
Animas Corporation is recalling 1,938 Vibe Insulin Infusion Pumps because keypad wear over time contributes to damage. The recall covers units distributed in France, Italy, Sweden, and the UK.
Product
Animas Vibe Insulin Infusion Pump and System. These products are indicated for continuous subcutaneous infusion of insulin for the treatment of insulin-requiring diabetes.
Category
Medical Device
Distribution
0 states
SevereFDA (Devices)·Z-0086-2015·2014-10-29
Siemens Mammomat Inspiration Mammography Systems Recalled for Safety Switch Defect
Siemens is recalling three Mammomat Inspiration mammography systems because a safety switch defect may allow the needle positioning device to move during a biopsy.
Product
Siemens Mammomat Inspiration mammography systems. The Mammomat Inspiration system is intended for mammography exams, screening, diagnosis, and stereotactic biopsies under the supervision of medical professionals. Mammographic images can be interpreted by either hard copy film
Category
Medical Device
Distribution
3 states
HighNHTSA·14V664000·2014-10-22
Spartan Gladiator Recall: Engine Cooling Fan May Break and Separate
Spartan Motors is recalling 2010-2015 Gladiator vehicles because the engine cooling fan may break during severe vibration, posing an injury risk if the hood is open.
Product
SPARTAN — SPARTAN GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0079-2015·2014-10-22
ArjoHuntleigh Recalls Spreader Bars for Ceiling Lifts Due to Hook Flexibility
Arjo, Inc. is recalling 363 spreader bars for the Maxi Sky 2 Ceiling Lift because the hooks are too flexible to securely hold sling loops.
Product
Medium 2-Hooks Spreader Bar for use with Loop Slings, sizes small, medium and large on the Maxi Sky 2 Ceiling Lift; Model 700-19425. Intended to be used for general transfers in hospitals.
Category
Medical Device
Distribution
5 states
HighNHTSA·14E068000·2014-10-10
Eaton Fuller 365mm Clutch Recall for Disengagement Failure
Eaton is recalling 574 Fuller 365mm clutches manufactured in 2014 due to a defective bearing that may prevent disengagement, increasing crash risk.
Product
POWER TRAIN:CLUTCH ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2737-2014·2014-10-08
Zimmer Recalls Persona Knee System Female Screws Due to Stripping Risk
Zimmer, Inc. is recalling 16,380 units of Persona The Personalized Knee System 2.5 mm Female Screws due to potential stripping of the hex driver when used in cortical bone.
Product
Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation, single use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2713-2014·2014-10-08
Siemens Symbia Intevo SPECT/CT Systems Recalled for Rubber Isolator Aging
Siemens Medical Solutions is recalling 48 Symbia Intevo SPECT/CT systems because a rubber isolator may degrade over time, potentially leading to drive belt rupture.
Product
The Symbia Intevo series consists of the Intevo 16, Intevo 6 and Intevo 2. This manual also describes the Symbia Intevo Excel. The Symbia Intevo series integrates state-of-the-art SPECT and high quality spiral CT to provide precise attenuation correction and anatomical mapping. T
Category
Medical Device
Distribution
40 states
HighFDA (Devices)·Z-2731-2014·2014-10-08
Intuitive Surgical Recalls da Vinci Xi Patient Side Carts Due to Sensor Failure
Intuitive Surgical is recalling 75 da Vinci Xi Patient Side Carts because a motor sensor failure can occur after a mid-procedure restart.
Product
ASSEMBLY, PATIENT SIDE CART, PS4000 used with the da Vinci Xi Surgical System. Product Usage: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Ins
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0009-2015·2014-10-08
Gendex eXpertDC Intraoral X-Ray Recall for Spring Link Failures
Gendex Corp is recalling 651 eXpertDC intraoral x-ray units worldwide because spring link components in the articulated arm assembly broke during normal assembly.
Product
eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch reach; eXpert DC, CN, 55 Inch reach; eXpert DC, WW, 75 Inch reach; eXpert DC, WW, 65 Inch reach; eXpert DC, WW, 55 Inch reach; OEM Arm Assembly w/o cables; Assy, Articulated Arm & Tubehead, eD
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2735-2014·2014-10-08
Nanosphere Verigene BC-GP Kit Extraction Tray Recall
Nanosphere is recalling Verigene BC-GP Kit extraction trays because a specific lot may cause processing errors and tips to drop into the processor.
Product
Verigene BC-GP Kit (Catalog number 20-005-018); 1) 20 Verigene BC-GP Test Cartridges; are qualitative multiplexed in vitro diagnostic tests for simultaneous detection and identification of selected gram-positive (BC-GP) and gram-negative (BC-GN) bacteria and resistance markers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2712-2014·2014-10-08
Siemens Symbia T Series Medical Imaging Systems Recalled for Rubber Isolator Defect
Siemens is recalling 1,039 Symbia T Series SPECT/CT systems because a rubber isolator may degrade, potentially leading to drive belt rupture.
Product
The Symbia T Series consists of the T16, T6, T2, and T. The Symbia T integrates state-of-the-art SPECT and high quality spiral CT to provide precise attenuation correction and anatomical mapping. The system can also be used as a complete clinical SPECT system for general purpose,
Category
Medical Device
Distribution
40 states
HighFDA (Devices)·Z-2693-2014·2014-10-01
ArjoHuntleigh Recalls Minstrel Mobile Passive Hoists Due to Bolt Failure
ArjoHuntleigh is recalling 18 Minstrel mobile passive hoists because a bolt under the scale may unscrew, posing a risk of the spreader bar detaching during use.
Product
Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting and transporting adult residents on horizontal floors in hospitals, nursing homes or other health care facilitates. The Minstrel device aids in the lifting, transfer and lowering to saf
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14754·2014-09-30
Husqvarna Recalls Craftsman Push Mowers Due to Injury Hazard
Husqvarna is recalling about 700 Craftsman push mowers sold at Orchard Supply Hardware because the engine control lever can fail, posing an injury risk.
Product
Push lawn mowers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·14V601000·2014-09-26
Altec DC1317 Wood Chippers Recalled for Cutting Disc Detachment Risk
Altec is recalling 2011-2014 DC1317 wood chippers because fasteners may fail, causing the cutting disc to detach and injure operators.
Product
ALTEC — ALTEC DC1317
Category
Consumer Product
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2656-2014·2014-09-24
Zenith Slide W-I-D-E Long Term Care Bed Recall for Head Deck Failure
GF Health Products is recalling 1,941 Zenith Slide W-I-D-E Long Term Care Beds because the head deck may fail to elevate during normal operation.
Product
Zenith Slide W-I-D-E Long Term Care Bed, Model(s) APS98674, APS9867406, APS986741, APS986742, ZG58674, ZG78674, ZZ78674, ZZ98674, and ZZ98774. Designed for use within an institutional healthcare environment (i.e. assisted living, skilled nursing, transitional care, rehabilitat
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2616-2014·2014-09-17
Pioneer Surgical Technology Recalls Streamline MIS Spinal Fixation System Fixed Rod Holders
Pioneer Surgical Technology is recalling nine Streamline MIS Spinal Fixation System Fixed Rod Holders because they failed to lock onto the spinal rod.
Product
Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE, Rx only The Streamline MIS Spinal Fixation System is intended for posterior, noncervical pedicle fixation, T1-S2. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2610-2014·2014-09-17
Ethicon Recalls PROXIMATE Skin Staplers Due to Unformed Staple Risk
Ethicon Endo-Surgery Inc is recalling PROXIMATE skin staplers because a non-conforming component may cause the device to fire an unformed staple.
Product
PROXIMATE Skin Stapler. PROXIMATE RH Rotating-Head Skin Stapler (Model PRR35), PROXIMATE PX Fixed-Head Skin Stapler (Model PXR35), Bulk/Non-Sterile PROXIMATE RH Rotating-Head Skin Stapler (Model CK 117), and Bulk/Non-Sterile PROXIMATE PX Fixed-Head Skin Stapler (Model CK 158
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2613-2014·2014-09-17
Baxter Recalls Buretrol Solution Sets Due to Chamber Separation
Baxter Healthcare is voluntarily recalling specific lots of Buretrol Solution Sets because the burette chamber may separate from the drip chamber.
Product
***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 Injection Sites Male Luer Lock Adapter with***Retractable Collar***Fluid path is Sterile, Nonpyrogenic***Indications for Use: For the administration of fluids from a container into
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2562-2014·2014-09-10
Hill-Rom Affinity Four Birthing Bed Recall for Latch Mechanism Defect
Hill-Rom is recalling 13,000 Affinity Four Birthing Beds because the attachment latch mechanism can bend, potentially causing the foot section to fail and resulting in user injury from a fall.
Product
Affinity¿ Four Birthing Bed, Product Usage: Product is intended to be used as birthing beds for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2556-2014·2014-09-03
Cordis EMPIRA NC RX PTCA Dilatation Catheter Recalled for Balloon Defect
Cordis Corporation is recalling 250,000 EMPIRA NC RX PTCA Dilatation Catheters because the balloon cover may be difficult to remove, potentially causing the balloon to burst or the shaft to separate during use.
Product
Cordis EMPIRA NC RX PTCA Dilatation Catheter
Category
Medical Device
Distribution
40 states