Medtronic Physio Control Corp DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor.
Brand
Medtronic Physio Control Corp
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Part numbers: VLP12-09-000031 through VLP12-09-000048. Serial numbers: 1563 through 5232 (non-contiguous)
Medtronic Physio Control Corp is recalling DC Power Adapter for use with the LIFEPAK 12 defibrillator/monitor. due to The DC Power Adapter may fail to charge LIFEPAK NiCd 2.4 AH batteries used with the LIFEPAK 12 defibrillator/monitor.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The DC Power Adapter may fail to charge LIFEPAK NiCd 2.4 AH batteries used with the LIFEPAK 12 defibrillator/monitor.
Recommended Action
Per FDA guidance
On 5/5/04 the firm issued a letter to consignees advising of the problem and that a service representative will contact them regarding replacement of the DC Power Adapter.
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