repair available Recalls

64 recalls tagged with “repair available”.

Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH Recalls 15,517 FLS Foot Locking Plates System and Hallux Osteotomy Plates Over MRI Heat‑

I.T.S. GmbH recalled 15,517 FLS Foot Locking Plates System and HOL Hallux Osteotomy locking plates distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than previously reflected in the IFU. Patients and healthcare providers should stop using this device immediately and follow the recall instructions from:

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Recalled 11 Pelvic Reconstruction System PRS Components for MRI Heating Risk (2026)

ITS GmbH recalled 11 Pelvic Reconstruction System PRS components after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions than described in the IFU. The recall covers Fixation Screw 70312 and Spike short 70314. Healthcare providers and patients should stop using the devices and follow the manufacturer’s recall instructions provided by email.

I.T.S. GmbH
Updated MRI
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Recalled Matrix Retail T30 (TM729) Treadmill
HIGH
CPSC

Johnson Health Tech Expands Treadmill Recall Over Fire Hazard

Johnson Health Tech expanded its recall of Matrix and Vision treadmills due to fire hazards. The affected models include T30, TF30, T50, TF50, T75, and others. Consumers should stop using these treadmills immediately and check for a power cord bracket.

Johnson Health Tech Expands
The power
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Health & Personal Care
HIGH
FDA DEVICE

Roche Cobas Pro 1,261-Unit Recall Over Spline-Calibration Error (2026)

Roche Diagnostics issued a nationwide recall of 1,261 Cobas Pro systems with cobas c 503 units in the United States. A software defect can cause erroneous, non-monotonic calibrations for spline-type assays. Labs should stop using the devices immediately and follow the manufacturer's recall instructions.

Roche Diagnostics Operations
Software defect,
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

GE Healthcare recalled 250 Centricity Universal Viewer Zero Footprint Client units distributed worldwide after finding a risk that patient information may not match displayed images in certain workflows. The issue affects ZFP v6.0 SP11.6, SP11.6.0.1 and SP11.6.1 when Patient Timeline is installed. Hospitals should stop using affected units and await instructions from GE Healthcare.

GE Healthcare
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System Recall Expands to 55 Units in 5 Countries (2026)

Olympus Corp. of the Americas recalls 55 ShockPulse-SE Lithotripsy System units distributed internationally. Mis-wired component may create noise on the power supply and ultrasonic circuit. Hospitals and providers should stop using the device immediately and follow recall instructions. Notify Olympus or your healthcare provider for guidance.

Olympus
Mis-wired component-the
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Recalled DR Power Equipment walk-behind leaf vacuum
MEDIUM
CPSC

DR Power Equipment Expands Leaf Vacuum Recall Over Laceration Hazard

DR Power Equipment recalled walk-behind and tow-behind leaf vacuums after reports of laceration hazards. The recall affects multiple model numbers sold from September 2014 to June 2025. Consumers should stop using these vacuums immediately and seek repairs.

Generac Power Systems Inc., of Waukesha, Wisconsin
Pieces from
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Health & Personal Care
LOW
FDA DRUG

Encon Safety Products Recalls AQ 120 GFEW Aquarion Preserved Cartridges in 2026

Encon Safety Products recalls AQ 120 GFEW Aquarion Preserved Cartridges sold nationwide through multiple retailers. The recall cites cGMP deviations in manufacturing. Stop using the product immediately and follow recall guidance from Encon Safety or your healthcare provider.

Encon Safety Products
cGMP deviations.
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Recalled MP2 Model of Amp Smart Fitness Machine
MEDIUM
CPSC

Amp Fit Recalls Smart Fitness Machines Over Laceration Hazard

Amp Fit recalled its MP2 model Smart Fitness Machine on December 18, 2025. The device poses a laceration risk due to an improperly locking arm. Consumers should stop using the machine immediately and contact Amp Fit for a free inspection and repair.

Amp Fit
The arm
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Recalled Electra Chandelier, Model No. 9000-1234
MEDIUM
CPSC

Currey & Company Recalls Electra Chandeliers Due to Fall Hazard

Currey & Company recalled all Electra Chandeliers and Electra Three Tier Chandeliers on December 18, 2025 after discovering a ceiling mount defect. This defect could cause the fixtures to fall unexpectedly, posing an impact injury risk. Consumers should stop using these chandeliers immediately and contact the company for repairs.

Currey & Company
The component
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical Recalls 2,095 da Vinci S, Si EndoWrist Tenaculum Forceps Instrument (2025)

Intuitive Surgical recalled 2,095 units of the da Vinci S, Si EndoWrist Tenaculum Forceps Instrument distributed nationwide in the United States and in multiple countries after reports of frayed or broken pitch cables. The defect can compromise instrument control during surgery. Hospitals and surgeons should stop using the device immediately and follow recall instructions from Intuitive Surgical.

Intuitive Surgical
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Intuitive Surgical da Vinci S, Si Grasping Retractor Instrument Recalled for 2,660 Units (2026)

Intuitive Surgical recalled 2,660 da Vinci S/Si Grasping Retractor Instruments worldwide after increased complaints of broken or frayed grip cables. The devices transmit motion from input disks to the distal tip and are used in robotic surgery. Hospitals and surgical centers should stop using the device immediately and follow recall instructions from the manufacturer.

Intuitive Surgical
Due to
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Recalled Grizzly Industrial 15” 3HP Heavy-Duty Planer
MEDIUM
CPSC

Grizzly Industrial Recalls Heavy-Duty Planers Due to Laceration Risk

Grizzly Industrial recalled all 15" 3HP heavy-duty planers with model number G0815 on December 4, 2025. The planers pose impact and laceration hazards due to a defect that allows the chip breaker to contact the cutterhead blades. Consumers should stop using the planers immediately and contact Grizzly for a free repair kit.

Grizzly Industrial
The chip
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Health & Personal Care
HIGH
FDA DEVICE

Affixus Femoral Nailing System Recalled Over Fracture Risk

Affixus recalled its Antegrade Femoral Nailing System on December 2, 2025, due to a potential implant fatigue fracture risk. The recall affects 22 units distributed nationwide in 14 states. Patients should stop using the affected devices immediately to avoid serious health risks.

Zimmer
Affected implants
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Health & Personal Care
HIGH
FDA DEVICE

Olympus ShockPulse-SE Lithotripsy System Recalled for 602 Reusable Probes (2025)

Olympus Corporation of the Americas recalls 602 ShockPulse-SE Lithotripsy System reusable probes worldwide to hospitals. The recall cites a blinking generator that may fail to recognize the transducer and damage the transducer plug or generator receptacle. Hospitals and patients should stop using SPL-SR probes immediately and follow manufacturer recall instructions.

Olympus
Ongoing investigations
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Recalled STIHL BR 800 X Magnum Backpack Blower
MEDIUM
CPSC

STIHL Recalls BR 800 Backpack Blowers Due to Laceration Hazard

STIHL recalled the BR 800 Magnum backpack blower on November 6, 2025, after discovering a laceration hazard. The recall affects models X and C-E with specific serial numbers. Consumers should stop using the product immediately and seek inspection and repair.

STIHL Incorporated, of Virginia Beach, Virginia
The fan
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Recalled Peloton Original Series Bike+ Model PL02
MEDIUM
CPSC

Peloton Recalls Original Series Bike+ Over Fall Hazard

Peloton recalled Original Series Bike+ models due to a fall hazard. The recall affects units with model number PL02 and serial numbers starting with "T." Consumers should stop using the bikes immediately and contact Peloton for a free repair.

Peloton
The bike's
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Recalled Milwaukee M18 FUEL Top Handle Chainsaw
MEDIUM
CPSC

Milwaukee Tool Recalls M18 FUEL Chainsaws Due to Laceration Hazard

Milwaukee Tool recalled M18 FUEL Top Handle Chainsaws due to a laceration hazard. The recall affects approximately 10,000 chainsaws sold since January 2023. Consumers should stop using the product immediately and contact Milwaukee Tool for a free repair.

Milwaukee Electric Tool Corp., of Brookfield, Wisconsin
The recalled
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Recalled Vaast A/1 bicycle
MEDIUM
CPSC

Super Wheels Recalls Vaast A/1 Bicycles Over Fall Hazard

Super Wheels recalled Vaast A/1 bicycles on October 16, 2025, after discovering a fall hazard. The recall affects 35 bicycle models and 15 frames sold in various colors. Consumers should stop using the bicycles immediately and contact the company for a replacement.

Super
The bicycle
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Recalled E-Z-GO Valor PTV
HIGH
CPSC

Textron E-Z-GO Recalls Personal Vehicles Over Fire Hazard

Textron E-Z-GO recalled personal transportation vehicles due to a fire hazard. The recall affects RXV Freedom and Valor models from 2020 to 2025. Consumers should stop using these vehicles immediately.

Textron E-Z-GO LLC, of Augusta, Georgia
The recalled
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Tag Statistics

Total Recalls
64

Related Tags

burn riskelectrical hazardimmediate actionstop use immediatelyreplacement availablefda regulatedcpsc regulatedreturn for refundfire hazardadult productelectronicmandatory standard violation