Medtronic Emergency Response Systems, Inc. standard (hard) paddles used with the LIFEPAK 12 defibrillator/monitor series. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
standard (hard) paddles used with the LIFEPAK 12 defibrillator/monitor series.
Brand
Medtronic Emergency Response Systems, Inc.
Lot Codes / Batch Numbers
Standard Hard Paddles part number: 3006228-013 and below
Products Sold
Standard Hard Paddles part number: 3006228-013 and below
Medtronic Emergency Response Systems, Inc. is recalling standard (hard) paddles used with the LIFEPAK 12 defibrillator/monitor series. due to Potential for voltage pins in connector of therapy cable to break.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for voltage pins in connector of therapy cable to break.
Recommended Action
Per FDA guidance
On 9/2/05 the firm issued letters dated September 2005 to their customers. The letters state the problem, advise the cables and/or connectors will be replaced, and emphasize daily inspection and testing,
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