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  1. FDA Recalls
  2. ›Device Recalls

FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification
AllClass IClass IIClass III
Status
AllOngoingCompletedTerminated
Date
All timePast 30 daysPast 12 months

Showing 321–340 of 1,000 recalls

Class IOngoing

Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide therapeutic benefit to those affected with advanced heart failure. In service, the LVAS assumes some or all of the workload of the left ventricle, thereby restoring the patient's systemic perfusion while palliating the underlying pathology. The LVAS features a Left Ventricular Assist Device (LVAD), a blood pump intended for long-term implantation in such patients, an extracorporeal Controller, plus all of the features, controls, attachments, interfaces, power sources, supporting equipment, labeling, and tools required to achieve the desired therapeutic benefit. The HeartMate II Left Ventricular Assist System is an axial-flow, rotary ventricular assist system that generates flows up to 10 liters per minute (lpm). One end of the Left Ventricular Assist Device is attached to the apex of the left ventricle; the other end of the device connects to the ascending aorta. The Left Ventricular Assist Device diverts blood from the weakened left ventricle and propels it to the aorta. A small external computer, the System Controller, monitors system operation. A driveline, which passes through the patient s abdomen, connects the implanted pump to the System Controller. The system is powered by a Power Module or Mobile Power Unit (MPU) that is connected to an AC electrical outlet, or by two HeartMate 14 Volt Lithium-Ion batteries. The LVAS may be used in any of two configurations. First, line power may be utilized through the Power Module or the Mobile Power Unit (MPU) to run the LVAD indefinitely, convenient for sedentary or sleeping periods. Second, portable Battery power may be utilized for limited periods, convenient for active periods. The MPU AC power cord is distributed either as part of the complete MPU device package or as a standalone accessory. Component: Yes, the MPU is a component of the HeartMate 3 and HeartMate II Left Ventricular Assist Systems.

Thoratec LLC

Due to misaligned V-Lock feature on the Mobile Power Unit power cords, which prevents the locking mechanism from properly engaging with the Mobile Power Unit and may cause unintended disconnect.

June 23, 2025 · DeviceView details →
Class IOngoing

Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX

Baxter Healthcare Corporation

Certain Spectrum infusion pumps may have an incorrect version of software.

June 20, 2025 · DeviceView details →
Class IOngoing

Baxter SIGMA Spectrum Infusion Pump V8, Model Number 35700BAX2

Baxter Healthcare Corporation

Certain Spectrum infusion pumps may have an incorrect version of software.

June 20, 2025 · DeviceView details →
Class IOngoing

i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.

Intersurgical Inc

Potential for faulty devices as a result of depleted batteries.

June 17, 2025 · DeviceView details →
Class IOngoing

SafeStar 90 Plus Filter. Bidirectionally breathing system filter.

Draeger, Inc.

Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.

June 16, 2025 · DeviceView details →
Class IOngoing

SafeStar 55 Plus Filter. Bidirectionally breathing system filter.

Draeger, Inc.

Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.

June 16, 2025 · DeviceView details →
Class IOngoing

SafeStar 60A Plus Filter. Bidirectionally breathing system filter.

Draeger, Inc.

Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.

June 16, 2025 · DeviceView details →
Class IOngoing

HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.

Draeger, Inc.

Reports of slow increase of CO2-curve when gas sample is taken from the gas sampling port of filters.

June 16, 2025 · DeviceView details →
Class IOngoing

Bravo CF capsule delivery device, designed to place and attach a pH monitoring capsule to the esophagus using endoscopic or manometric guidance, Product Number FGS-0635 (5 pack) and FGS-0636 (1 pack)

Given Imaging Ltd.

It has been determined that misapplied adhesive on the Bravo CF capsule delivery device may lead to its malfunction. Specifically, the misapplied adhesive may prevent the capsule from attaching to the patient's esophagus or detaching from the delivery device.

June 3, 2025 · DeviceView details →
Class IOngoing

Hamilton C6 REF 160021 (ESM Board PN 10144626 UDI-DI code: 76300028PN160021ZW Hamilton C6 is a ventilator intended to provide positive pressure ventilatory support to adults and pediatrics and optionally infants and neonates.

Hamilton Medical AG

A mechanical defect on a printed circuit board (PCB) as a result of PCB separating process. This defect might cause the ventilator to either fail at startup (no patient involvement) or during the use of the device enter ambient state, resulting in an interruption of ventilation.

June 3, 2025 · DeviceView details →
Class IOngoing

Servo-u Ventilator System. Model Number: 6688600.

Maquet Critical Care AB

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

May 30, 2025 · DeviceView details →
Class IOngoing

Servo-n Ventilator System. Model Number: 6694800.

Maquet Critical Care AB

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

May 30, 2025 · DeviceView details →
Class IOngoing

Hillrom LikoScale component, Product Code 3156232, used with the following adapter kits for patient lifts: 1) LikoScale 200 Accessory - Product Code 3156225; 2) LikoScale 350 Accessory - Product Code 3156228; 3) LikoScale 400 Accessory - Product Code 3156226.

Baxter Healthcare Corporation

The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.

May 30, 2025 · DeviceView details →
Class IOngoing

Hillrom Q-Link 13 component, Product Code 3156509, used with the following Mobile Patient Lifts: 1) Uno 102 EE Mobile lift - Product Code 2010004; 2) Viking L Mobile lift - Product Code 2040044; 3) Viking XL Mobile lift - Product Code 2040043; 4) Viking M Mobile lift - Product Code 2040045A; 5) Viking S Mobile Lift - Product Code 2040006; 6) Viking XS Mobile Lift - Product Code 2040007; 7) LikoLight Mobile lift - Product Code 2030001. .

Baxter Healthcare Corporation

The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.

May 30, 2025 · DeviceView details →
Class IOngoing

Servo-u MR Ventilator System. Model Number: 6888800.

Maquet Critical Care AB

Potential for inaccurate measurement of the patient circuit compliance during the patient circuit test due to combination of incorrect pre-use leakage test and use of an incorrect active humidifier.

May 30, 2025 · DeviceView details →
Class IOngoing

MicroMyst Applicator, Box of 5. Consisting of a multilumen applicator and filtered line for use with the Integra Flow Source for the controlled application of two liquids.

Integra LifeSciences Corp. (NeuroSciences)

Lack of sterility assurance.

May 23, 2025 · DeviceView details →
Class IOngoing

Extended Tip Applicator, 15 CM, Box of 5.

Integra LifeSciences Corp. (NeuroSciences)

Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.

May 22, 2025 · DeviceView details →
Class IOngoing

Extended Tip Applicator, 8CM, Box of 5.

Integra LifeSciences Corp. (NeuroSciences)

Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.

May 22, 2025 · DeviceView details →
Class IOngoing

Extended Tip Applicator 8CM, Box of 1.

Integra LifeSciences Corp. (NeuroSciences)

Devices contain potentially out-of-specification levels of endotoxins and lack of sterility assurance.

May 22, 2025 · DeviceView details →
Class IOngoing

Newport HT70 Ventilator, REF: HT70M-JP-NA, HT70M-CN-NA, HT70M-ES-EU, HT70M-PT-BR, HT70M-SY-EU, HT70M-WW-EU, HT70M-WW-NA, HT70-SY-EU. Newport HT70Plus Ventilator, REF: HT70PM-ES-EU, HT70PM-ES-NA, HT70PM-JP-NA, HT70PM-PT-BR, HT70PM-SY-AS, DLHT70PM-WW-NA, HT70PM-SY-NA, HT70PM-SY-UK, HT70PM-WW-EU, HT70PM-WW-UK, HT70PM-SY-EU, HT70PM-WWNA. HT70-2 CONTROL BOARD ROHS X1, REF: GR105796. HT70P CONTROL BOARD ROHS X1, REF: GR105795. HT70 Conversion Kit, REF: GRFSKHT70M-2.

Covidien

Ventilator Printed Circuit Board Assembly may have two separate capacitors that may fail, which may result in the ventilator either shutting down during use, thus necessitating use of an alternate form of ventilation, or the shutdown alert alarm fails to alarm effectively during shut down, which may result in respiratory failure, hypoventilation, low oxygen saturation, hypoxia, treatment delay.

May 21, 2025 · DeviceView details →
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