Medtronic Physio Control Corp LIFEPAK CR Plus defibrillator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LIFEPAK CR Plus defibrillator
Brand
Medtronic Physio Control Corp
Lot Codes / Batch Numbers
All serial numbers below 31058753
Products Sold
All serial numbers below 31058753
Medtronic Physio Control Corp is recalling LIFEPAK CR Plus defibrillator due to Defibrillation therapy may be delayed or not delivered for persons needing defibrillation therapy.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Defibrillation therapy may be delayed or not delivered for persons needing defibrillation therapy.
Recommended Action
Per FDA guidance
On 5/23/03, the firm issued a recall letter to customers advising of the malfunctions and instructions to check the device to assure it is ready for use. Service representatives will visit the customer sites and replace the flex circuit in all affected devices.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026