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.

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.

151–175 of 1703

HighFDA (Devices)·Z-1906-2023·2023-06-21
Prosthetic Socket Ratchet Locking Systems Recalled for Suspension Loss Risk
Mechanical locking devices for prosthetic sockets may develop accelerated wear that causes the attachment pin to disengage, potentially leading to loss of prosthetic suspension and falls.
Product
Icelock 125 Ratchet, REF: L-125000; Icelock 600XM Ratchet, REF: L-621200; Icelock 621 Ratchet, REF: L-621000; Icelock 621 Ratchet Adaption Kit, REF: L-621100; Ratchet Lock Body, REF: L-692020
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-1668-2023·2023-06-07
Medical Device Recall: X-Ray Detector Drive Shaft May Break
The FDA is recalling 32 X-ray detector units due to a potential drive shaft failure that could cause uncontrolled detector movement. Affected units are distributed in 10 US states.
Product
Intelli-C, Right side suspended Tabletop, REF: 03400000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1669-2023·2023-06-07
X-Ray Machine Detector May Move Unexpectedly Due to Drive Shaft Failure
FDA recalls the Intelli-C X-Ray machine's left side suspended tabletop model due to potential drive shaft failure in the detector lift mechanism, which could cause uncontrolled detector movement.
Product
Intelli-C, Left side suspended Tabletop, REF: 03400010
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V326000·2023-05-04
Altec Recalls 2017-2022 Digger Derricks Due to Missing Hardware
Altec is recalling 2017-2022 Digger Derricks because missing hardware may allow the auger extension bar to detach, increasing injury risk.
Product
ALTEC — ALTEC DIGGER DERRICK
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1424-2023·2023-05-03
Endoscopic Forceps May Fail to Open When Shaft Bent
Surgical grasping forceps may fail to open when the endoscope shaft is bent, potentially affecting their use during endoscopic procedures.
Product
FLEX. GRASP. FORCEPS 5FR WL 550MM, Product Number 8735.685
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1414-2023·2023-04-26
Samsung GM85 Digital X-ray Imaging System Arm Latch Failure
NeuroLogica Corporation recalls 935 Samsung GM85 digital X-ray systems due to a faulty arm latch in the column support that could allow the arm to fall, creating a risk of bodily injury.
Product
Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·23E035000·2023-04-24
Dana Spicer Ultimate Dana 60 Axle Recall for Jeep Wrangler
Dana Incorporated is recalling Spicer Ultimate Dana 60 Bracketless Crate Axles for Jeep Wranglers because a suspension bracket may prevent sufficient lubrication from reaching the pinion tail bearings.
Product
POWER TRAIN:AXLE ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1208-2023·2023-03-08
Dental Handpieces Recalled Due to Detachable Screw Component Risk
Coltene Whaledent Inc is recalling SciCan STATIS SL S10001 dental handpieces because the screw connection between the turbine head and push button may loosen and fall off, creating a risk of swallowing or inhaling these parts.
Product
SciCan STATIS SL S10001 Dental Handpieces-Intended for the removal of carious material, reducing hard tooth structure, cavity preparation, finishing tooth preparations, restorations and for polishing teeth. Model Number: S10001
Category
Medical Device
Distribution
Distributed nationwide
ModerateCPSC·23131·2023-02-23
SCARPA F1 Ski Boots Recalled for Fall Hazard
SCARPA North America is recalling about 770 F1 LT and F1 GT ski boots manufactured in 2022. Screws attaching the ski/walk mechanism can loosen or fall out, causing the mechanism to malfunction and posing a fall hazard.
Product
F1 LT and F1 GT Ski Boots
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0277-2023·2023-02-22
Orthopedic Implant Bolts Recalled Due to Breakage Risk in Bone Correction
OrthoPediatrics has recalled Orthex Large Bone Shoulder Bolts due to breakage risk that may disrupt bone correction and healing. Affected units were distributed in the United States and internationally.
Product
Orthex Large Bone Shoulder Bolt, model no. AS-17
Category
Medical Device
Distribution
0 states
HighFDA (Devices)·Z-1135-2023·2023-02-22
Potential Gantry Locking Mechanism Defect in SIEMENS Biograph mCT PET Scanners
The SIEMENS Biograph mCT PET scanner has a potential issue with the locking mechanism that secures the gantry. Six units distributed worldwide including the US, Japan, Chile, and Australia are affected.
Product
SIEMENS Biograph mCT: a) Flow 64-4R Seismic, b) S(40)-3R Seismic, c) S(64)-3R Seismic, d) S(40)-4R Seismic, e) S(64)-4R Seismic, f) S(20)-3R Mobile
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1058-2023·2023-02-15
GE Nuclear Medicine 600/800 Systems Recalled for Detector Fall Risk
GE Medical Systems is recalling 380 GE Nuclear Medicine 600/800 series diagnostic imaging systems worldwide due to potential failure in detector mitigation that could allow the detector to fall, risking life-threatening injury.
Product
GE Nuclear Medicine 600/800 series systems, specifically: a) 850, b) 850 / Dismount, c) 850 3/8 inch NM Gantry, d) 860 / Dismount, e) 860 3/8 inch NM Gantry, f) 860 5/8 inch NM Gantry, g) 860 BJ, h) NM 830 3/8 inch BJ, i) NM/CT 850 3/8 inch BJ, j) NM/CT 850 3/8 inch…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0956-2023·2023-01-25
ARTIS medical imaging systems recalled for mechanical connection failure
Siemens ARTIS pheno and ARTIS icono imaging systems are recalled because the mechanical connection between the tabletop and table base may fail. The recall affects 550 units distributed worldwide.
Product
ARTIS pheno, ARTIS icono biplane, and ARTIS icono floor
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0923-2023·2023-01-18
Adult Craniotome Attachment Recalled for Ball Bearing Failure Risk
The ANSPACH CRANI-A Adult Craniotome Attachment is recalled because ball bearings can separate during use or removal, creating an intra-operative hazard. The Anspach Effort, Inc. is recalling 6,059 units distributed nationwide and internationally.
Product
6.5 cm Pediatric Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-P Intended for cutting and shaping bone including the spine and cranium
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0738-2023·2022-12-28
Spinal implant insert may fail to disengage from vertebral body device
NuVasive's X-CORE 2 spinal implants may not disengage properly from the vertebral replacement device, potentially requiring revision surgery. About 2,031 devices worldwide are affected.
Product
X-CORE 2 Ti Core, Static. Part of the NuVasive X-Core Expandable VBR System used with spinal fixation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0479-2023·2022-12-21
Medical cot may experience unintended motion due to cable damage
Stryker's Power-PRO 2 surgical cot may lower unexpectedly due to damaged cables, risking soft tissue injuries to patients. The recall affects 465 units distributed in the US and internationally.
Product
Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V918000·2022-12-12
Prevost Recalls 2017-2018 X3-45 Motorcoaches Due to Engine Stop Button Defect
Prevost is recalling 2017-2018 X3-45 motorcoaches because the engine stop button may fail to stop the engine, increasing injury risk to service technicians.
Product
PREVOST — PREVOST X3-45
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0239-2023·2022-11-23
Operating Table Extension Tabletop May Drop, Creating Patient Fall Hazard
The back rest of Getinge operating table extension tabletops may drop unexpectedly, posing a fall hazard to patients. No injuries have been reported.
Product
Extension Tabletop for Operating Table System 1140, Model Nos. 1140.20F0 and 1140.20AN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0246-2023·2022-11-23
OneLIF Torque Limiting Adapter Recalled for Potential Locking Failure
Novapproach Spine is recalling OneLIF Torque Limiting Adapter components used in spinal surgery instruments because the adapter may not remain locked in the ratcheting handle once fully engaged. This could compromise surgical instrument function during use.
Product
OneLIF Torque Limiting Adapter, AO to 1/4 SQ, 2.25Nm Limit, Catalog #015-010-0000, a component of NovApproach Spine OneLIF Interbody System instrument kit, Catalog #OneLIF INS.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0243-2023·2022-11-23
EasyStand Bantam standing devices may fail to maintain upright position
Altimate Medical is recalling EasyStand Bantam Small and Extra Small standers due to a component defect that may prevent the leg assembly bracket from maintaining the non-supine position. No injuries have been reported.
Product
EasyStand Bantam, with the following sizes. a. Small; b. Extra Small. Used for assisting individual in standing.
Category
Medical Device
Distribution
7 states
HighFDA (Devices)·Z-0179-2023·2022-11-09
Allen Life Assist Beach Chair Adhesive Cure Failure Recall
Baxter Healthcare is recalling the Allen Life Assist Beach Chair due to adhesive on fasteners that may not cure correctly, potentially compromising the device's mechanical integrity during surgical procedures.
Product
Allen Life Assist Beach Chair, BCSSP-BEACH CHAIR , REF A-91501, #104002. For use with orthopaedic procedures using the Fowlers or beach chair position.
Category
Medical Device
Distribution
4 states
SevereFDA (Devices)·Z-0075-2023·2022-10-26
Iso-Gard Filter S Medical Gas Filters Recalled Due to Device Splitting Risk
TELEFLEX is recalling 355 units of Iso-Gard Filter S medical gas filters nationwide due to incidents of device splitting or detaching during use. The FDA classified this as a Class I recall.
Product
Iso-Gard Filter S, with Expandi-Flex, Tethered Cap, REF: a) 19261T, OUS only; b) 19262T, OUS only; c) 19272T, OUS only; Microbial medical gas filter, single-use,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0074-2023·2022-10-26
Medical Gas Filter Devices Recalled Due to Splitting and Detachment Risk
Teleflex is recalling Iso-Gard Filter S microbial medical gas filters that may split or detach during use. The recall affects 164 units distributed nationwide.
Product
Iso-Gard Filter S, Tethered Cap, REF: a) 19211T, OUS only; b) 19212T, OUS only; Microbial medical gas filter, single-use
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1815-2022·2022-10-05
Olympus POWERSEAL 5MM Electrosurgical Sealer Recalled Due to Loose Retention Ring
Olympus is recalling POWERSEAL 5MM electrosurgical sealers due to a component defect that may cause the rotation knob to loosen and delay surgical treatment.
Product
Olympus POWERSEAL 5MM, 44CM, CURVED JAW SEALER & DIVIDER, DOUBLE-ACTION Model Number: PS-0544CJDA. An electrosurgical device use in laparoscopic/minimally invasive or open surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V681000·2022-09-12
Commercial Trucks Recalled for Steering Shaft Component Failure
Daimler Trucks North America is recalling 2022-2023 Western Star 47X and 49X commercial trucks because the steering shaft's u-joint pinch bolt may detach, causing loss of steering control.
Product
WESTERN STAR — WESTERN STAR 49X, 47X
Category
Vehicle
Distribution
Distributed nationwide