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Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc. Recalls

All product recalls associated with Medtronic Emergency Response Systems, Inc..

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Recall Summary

Total Recalls

710

Past Year

Class I (Serious)

Most Recent

Dec 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 641–660 of 710 recalls

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

Premature battery depletion due to electrical component failure

FDAOct 5, 2006IN• Medtronic Emergency Response Systems, Inc.

Tosoh Bioscience Inc: TOSOH AIA-PACK FOLATE Calibrator Sets, six levels, Catalo...

Reports of low calibration rate value flags; Use of the recalled product may result in failure to calibrate the instrument

FDASep 1, 2006Nationwide• Tosoh Bioscience Inc

1...31 323334 35 36

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Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 external defibrillator/monitor

Devices with v38 system software do not display a ''LOW BATTERY: CONNECT TO AC POWER'' message when the monitor is on backup (DC) battery power and may shut down without warning.

FDAAug 30, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Edwards Lifesciences Llc One Edwards Way: EDWARDS VIGILANCE MONITORS (FORMERLY BAXTER VIGILANCE MON...

Edwards Lifesciences Vigilance monitors with software release 5.3 or earlier may improperly cause the monitor to deliver power to the Continuous Cardiac Output (CCO) catheter without alerting the user to this situation. This can result in overheating and thermal damage to the CCO catheter and serious patient injury.

FDAJun 21, 2006Nationwide• Edwards Lifesciences Llc One Edwards Way

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: ExacTrac Robotics, sold alone as Robotic Tilt Module cata...

During ExacTrac Robotics installation on the Varian Exact Couch, the couch height position indication is re-calibrated to read out the correct positions. This re-calibration could cause the eventual failure of the vertical lift mechanism of the couch, which might result in patient injury or death.

FDAJun 2, 2006Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Meridian Bioscience Inc: ImmunoCard toxins A & B kit, a rapid enzyme immunoassay f...

The product may produce non-specific reactions with negative specimens and/or the negative control reagent. These non-specific interactions may result in increased invalid test rates and/or positivity rates.

FDAJun 2, 2006Nationwide• Meridian Bioscience Inc

Edwards Lifesciences Research Medical, Inc.: Duraflo Treated Aortic Perfusion Cannula with plastic tip...

Due to potential embrittlement of the plastic tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: Aortic Perfusion Cannula with Metal Tip, 22 Fr. x 23 cm. ...

Due to potential embrittlement of the overmolded plastic portion of the metal tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Edwards Lifesciences Research Medical, Inc.: Aortic Perfusion Cannula with plastic tip, 22 Fr. x 28 cm...

Due to potential embrittlement of the plastic tip which may crack or separate during use.

FDAApr 18, 2006CA, CT, FL +7 more• Edwards Lifesciences Research Medical, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 defibrillator/monitor

Therapy connectors may have connector sockets that do not meet design specs - short drill depth. Interruption of the connections may cause unexpected, intermittent or complete loss of pacing and defibrillation functions.

FDAMar 22, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

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

FDAMar 22, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 20 automatic external defibrillator

LIFEPAK 20 may lock-up when attempting to power-up on DC within 2 seconds after removing AC power.

FDAMar 16, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK 500 automated external defibrillator (AED)

Component leads may have intermittent connection to the printed circuit board assembly pads - which could render the device inoperative.

FDAFeb 1, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK EXPRESS defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Medtronic Emergency Response Systems, Inc.: LIFEPAK CR Plus defibrillator

One of the printed circuit board assemblies may be contaminated with solder flux which can cause a short that may render the device inoperative.

FDAJan 31, 2006Nationwide• Medtronic Emergency Response Systems, Inc.

Cardiac Science Corporation: Powerheart AED G3 Automated External Defibrillator Model ...

Some Powerheart AED Model 9300A may contain a suspect electronic component and there is a remote likelihood that the function of this device may be interrupted during the charge.

FDAJan 27, 2006Nationwide• Cardiac Science Corporation

Tosoh Bioscience Inc: TOSOH ST AIA- PACK TT3, Lot FX17440, catalog #025...

The inner foil packs of AIA-PACK ST TT3, Lot FX17440 contain an incorrect expiration date of 10/2005. The outer box is labeled with the correct expiration date of 10/2006.

FDAJan 26, 2006GA, KS, TX +1 more• Tosoh Bioscience Inc

Integra LifeSciences Corp.: Selector Ultrasonic Integra Ultrasonic Aspirator System, ...

Additional Model 24kHz Tip Sets were inadvertently packaged with the incorrect 35kHz Neuro Flues. (2nd recall, same problem see Z-141-6)

FDANov 28, 2005Nationwide• Integra LifeSciences Corp.

Bombardier Outlander 800 ATV – Mechanical Risk (2005)

The recalled vehicles are model year 2006 Outlander 800 H.O. XT Bombardier ATVs. The model numbers affected are 2J6A and 2J6E. The model numbers are located in the serial number on the identification sticker under the seat. The ATVs have the words, "Bombardier" and "Rotax 800" on the fenders.

CPSCOct 11, 2005Nationwide• Bombardier Recreational Products Inc., of Valcourt, Providence of Quebec, Canada