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.

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 1704

HighFDA (Devices)·Z-0530-2015·2014-12-17
Abbott Healon EndoCoat Ophthalmic Device Recalled for Finger Grip Defect
Abbott Medical Optics is recalling Healon EndoCoat ophthalmic devices because the finger grip can dislodge, potentially causing eye trauma during surgery.
Product
Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate 0.85 mL 30 mg/mL Sterile A Solution Sterile EO Packaging and Cannula Product of USA Abbott Healon Duet Dual Pack 0.55 ml OVD 0.85 ml Healon EndoCoat OVD Contents: -one sterile syringe of…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0503-2015·2014-12-17
Snug Seat Recalls Crocodile Size 3 Walking Aids Due to Bolt Failure
Snug Seat Inc is recalling 726 Crocodile size 3 walking aids because bolts securing the handles could break, causing the handles to dislodge.
Product
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The Crocodile is a walking aid for children with disabilities, who need supplementary assistance with their daily walking. The Crocodile is available in three sizes and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0574-2015·2014-12-17
Zimmer Title 2 Bone Screw Remover Recalled for Weld Failure Risk
Zimmer, Inc. is recalling 14 Title 2 Bone Screw Remover instruments due to a risk that the weld may break during use, potentially delaying surgery.
Product
Zimmer Title 2 Bone Screw Remover Instrument, Part Number ET1093-01 Rx Only, Non-Sterile. The Screw Remover is a component of the Endius TITLE 2 Polyaxial Spinal System, used for posterior lumbar fusion procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0494-2015·2014-12-10
Aircraft Medical Recalls McGrath MAC2 Video Laryngoscope Blades
Aircraft Medical Limited is recalling McGrath MAC2 Video Laryngoscope Blades because the retaining clip may be difficult to engage, increasing the risk of the blade disconnecting during intubation.
Product
McGrath MAC2 Video Laryngoscope Blades Product supplied in box of 50 items, each individually peel-pouched and EtO sterilized. Product Usage: Single Use, sterile video laryngoscope blade for use with McGRATH MAC Video Laryngoscopes
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0428-2015·2014-12-03
Intuitive Surgical Recalls 8mm Large Needle Driver Instruments
Intuitive Surgical is recalling 509 8mm Large Needle Driver instruments due to potential surface degradation and accelerated mechanical wear caused by reprocessing deviations.
Product
8MM,LARGE NEEDLE DRIVER; Intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments.
Category
Medical Device
Distribution
8 states
HighFDA (Devices)·Z-0216-2015·2014-11-26
Silver Star Brands Recalls Transport Chair and Rollator Due to Wheel Failure
Silver Star Brands is recalling Transport Chair and Rollator units because the wheel assembly may fail, resulting in damaged wheels.
Product
Transport Chair and Rollator in 1, Model HE21630011 Burgundy and HE21630011 Blue. This is a walker/rolling chair. Used to assist injured and infirm people to walk or be ambulatory.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0182-2015·2014-11-19
Philips Allura Xper FD20C Recalled for Faulty Motion Controller
Philips Medical Systems is recalling two Allura Xper FD20C systems due to a faulty Automatic Motion Controller that may cause hazardous C-arc movement.
Product
Philips Medical Systems Allura Xper FD20C with software version R8.2.O System Code: 722035. The Allura Xper FD series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and…
Category
Medical Device
Distribution
2 states
SevereFDA (Devices)·Z-0210-2015·2014-11-19
Fisher and Paykel Infant Warmer Recall Due to Heater Head Breakage
Fisher and Paykel Healthcare is recalling IW900-Series Infant Warmers and spare parts because a broken nut may allow the heater head to swing and injure infants.
Product
Fisher and Paykel Healthcare (FPH) IW900-Series Infant Warmer Fisher and Paykel; Healthcare CosyCot and Kit Replacement Head Case Assembly It is designed to assist with the thermoregulation of infants weighing up to 10kg and is used by labor and delivery rooms and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0181-2015·2014-11-19
Philips Allura Xper FD20C Radiological Imaging Systems Recalled for Motion Controller Fault
Philips is recalling 22 Allura Xper FD20C radiological imaging systems due to a faulty Automatic Motion Controller that may cause hazardous movement of the C-arc.
Product
Philips Medical Systems Allura Xper FD20C Radiological Imaging with software version R8.2.O; System Code: 722028. The Allura Xper FD series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including…
Category
Medical Device
Distribution
2 states
HighFDA (Devices)·Z-0196-2015·2014-11-19
Steris 5085 Surgical Tables Recalled for Damaged Column Shrouds
Steris is recalling 5085 and 5085SRT surgical tables because column shrouds may become damaged, potentially preventing the table from raising or lowering.
Product
The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation.
Category
Medical Device
Distribution
36 states
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…
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-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
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
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…
Category
Medical Device
Distribution
3 states
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·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
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-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…
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.…
Category
Medical Device
Distribution
40 states
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…
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