Product Recalls
This page contains information from the FDA on recalls related to Automated External Defibrillators and other CPR related products.
Class 1 Recall: Physio-Control, Inc, LIFEPAK CR Plus Automated External Defibrillators
- Date Recalled: September 16, 2009
- Product: LIFEPAK CR Plus Automated External Defibrillators
- Reason for Recall: An extremely humid environment may cause the affected devices to improperly analyze the heart rhythm and may cause the device to delay or fail to deliver therapy.
- Link to FDA website
Class 1 Recall: Welch Allyn AED 10 Automatic External Defibrillator (AED) and MRL Jumpstart AED
- Date Recalled: December 15, 2008
- Product: Welch Allyn AED 10 Automatic External Defibrillator (AED) and MRL Jumpstart AED
- Reason for Recall: The device may expereience low defibrillation energy delivery, unexpected shutdown, and/or inadequate filtering of electromagnetic noise
- Link to FDA website
Class 1 Recall: ZOLL Medical Corporation, ZOLL AED Plus Defibrillator
- Date Recalled: February 12, 2009
- Product: ZOLL AED Plus Defibrillator
- Reason for Recall: The AED failed to deliver the defibrillation energy
- Link to FDA website
Class 1 Recall: Physio Control LifePak CR Plus Automated External Defibrillator (AED)
- Date Recalled: September 17, 2008
- Product: Physio Control LifePak CR Plus Automated External Defibrillator (Product #:3200731-003)
- Reason for Recall: The AED "shock" button may not function properly
If you have questions or need assistance in regards to this or other product recalls or upgrades, please contact us at nduclos@mcgregorems.org.
