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Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment Recalls

All product recalls associated with Medtronic Inc. Cardiac Rhythm Managment.

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Recall Summary

Total Recalls

606

Past Year

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 581–600 of 606 recalls

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync III Protect, model 7285 Dual Chamber Imp...

Medtronic marquis family of ICD and CRT-D devices having batteries manufactured prior to December 2003 that may experience rapid battery depletion due to a specific internal battery short mechanism. Once a short occurs, depletion can take place within a few hours to a few days, after which there is a complete loss of device function.

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Marquis VR, model 7230 Single Chamber Implantab...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync Marquis, model 7277 Dual Chamber Implant...

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FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync III Marquis, model 7279 Dual Chamber Imp...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Marquis DR, model 7274 Dual Chamber Implantable...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Maximo VR, model 7232 Single Chamber Implantabl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic InSync II Marquis, model 7289 Dual Chamber Impl...

FDAFeb 9, 2005Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 AED.

Potential to not detect patients at the low end of the patient impedance range.

FDAFeb 3, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Surgical Navigation Technologies, Inc: Stealth Station Cranial Application v.4.5

The Stealth Station Cranial Application Version 4.5 contains a software anomaly, which may present a hazard to the patient.

FDAJan 28, 2005AL, AZ, AR +20 more• Medtronic Surgical Navigation Technologies, Inc

Medtronic Emergency Response Systems, Inc.: LIFEPAK 12 defibrillator/ monitors biphasic

The LIFEPAK 12 biphasic defibrillator/ monitors may deliver inappropriate energy levels and fail to escalate energy levels when configured to do so.

FDAJan 15, 2005Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Inc, Neurological & Spinal Division: Model 8561 Lioresal (Baclofen injection) Intrathecal Refi...

Outer package of Lioresal Intrethecal Refill Kit, model 8561, identifies the kit to contain 1-20 ml ampule of baclofen injection for intrathecal administration, 500 mcg/ml (10 mg/20 ml). Lot N0016487 incorrectly contains 1-20 ml ampule of baclofen concentration 2000 mcg/ml (40 mg/20 ml).

FDANov 19, 2004Nationwide• Medtronic Inc, Neurological & Spinal Division

Medtronic Xomed, Inc.: Brand name: NIM EMG Endotracheal Tube ...

The firm received six reports of tubes with wires 'out of channel' two of which involved injuried patients. In one case in Germany it was reported that the patient had soreness of the throat and was discharged after four days. In the next case the patient had a tracheal wound. It was not clear what caused the wound.

FDAOct 29, 2004Nationwide• Medtronic Xomed, Inc.

Medtronic Inc. Cardiac Rhythm Managment: Medtronic CapSureFix Novus Lead Model 5076.

A specific lot of leads are labeled incorrectly. The leads are 45 cm in length and labeled as 52 cm lead length.

FDAOct 20, 2004Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc: Medtronic DLP VAD Venous Cannula for Ventricular Assist, ...

Spiral tip from DLP VAD cannula may be loose and potentially detach during use.

FDASep 15, 2004Nationwide• Medtronic Inc

Medtronic Inc, Neurological & Spinal Division: 8870 software application card versions AAA 02, BBB 04, B...

With the Model 8870 software application card versions AAA 02, BBB 04, BBC 02, and BBD 01, which is used in conjunction with the Model 8840 N'Vision Clinician Programmer, users may have mistakenly entered a periodic bolus interval into the minutes field, rather than the hours field, resulting in drug overdoses. This issue is limited to programming the SynchroMed and SynchroMed EL pumps.

FDAAug 24, 2004IN• Medtronic Inc, Neurological & Spinal Division

Medtronic Inc, Neurological & Spinal Division: The Model 8540 Catheter Access Port Kit is intended for u...

The sterile tray label for the Model 8540 Catheter Access Port kit may be incorrectly labeled with a Model 8551 Refill kit label. The outer box of the affected Model 8540 Catheter Access Port kit is labeled correctly and the component parts within the sterile tray are the correct components for a Model 8540 Catheter Access Port kit. The issue is limited to one lot of product: CS0293.

FDAJul 23, 2004IN• Medtronic Inc, Neurological & Spinal Division

Medtronic Inc, Neurological & Spinal Division: Synchromed II infusion pump

The opposite version serial numbers were assigned to 20mL and 40mL SynchroMed II Model 8637 pumps. This size-type indication is used by the programmer to identify the pump size and can cause a limitation in the useable fill volume on a 40 mL pump and could cause some confusion related to the size of a 20 mL pump which identifies itself as a 40 mL pump.

FDAMay 11, 2004Nationwide• Medtronic Inc, Neurological & Spinal Division

Medtronic Inc. Cardiac Rhythm Managment: Medtronic GEM DR Implantable Cardioverter Defibrillators,...

Some of the devices with suspect capacitors (high voltage capacitors associated with prior notifications in 1999 and in 2000) have had unexpected charge circuit time-outs or charge circuit inactive conditions as the battery voltage nears the level for Elective Replacement of the devices.

FDAApr 2, 2004Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Inc. Cardiac Rhythm Managment: Medtronic Micro Jewel II Implantable Cardioverter Defibri...

FDAApr 2, 2004Nationwide• Medtronic Inc. Cardiac Rhythm Managment

Medtronic Xomed, Inc.: Product is a surgical nasal/sinus surgical device labeled...

The curve in the shaft of the bur was only 15 degrees not the labeled 40 degrees.

FDAJan 29, 2004FL, ID, IN +12 more• Medtronic Xomed, Inc.