Medtronic Emergency Response Systems, Inc. LIFEPAK 20 defbrillator/monitor Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LIFEPAK 20 defbrillator/monitor
Brand
Medtronic Emergency Response Systems, Inc.
Lot Codes / Batch Numbers
Various, noncontiguous serial numbers. Part numbers: 3202487-xxxd and 3202488-xxx.
Products Sold
Various, noncontiguous serial numbers. Part numbers: 3202487-xxxd and 3202488-xxx.
Medtronic Emergency Response Systems, Inc. is recalling LIFEPAK 20 defbrillator/monitor due to The defibrillator may not operate if the device is turned on during an AC Loss Alert.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The defibrillator may not operate if the device is turned on during an AC Loss Alert.
Recommended Action
Per FDA guidance
On 6/17/05 the firm issued a medical device correction letter to customers advising of the problem, explained what to do if the situation occurs, and that a service representative will visit and install new software.
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