Medtronic Emergency Response Systems, Inc. Batteries used with the LIFEPAK 20 defibrillator/monitor Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Batteries used with the LIFEPAK 20 defibrillator/monitor
Brand
Medtronic Emergency Response Systems, Inc.
Lot Codes / Batch Numbers
Battery Product Part Number: 3200497-000 Battery lot codes: prior to 0539, lot codes: 05 265 or 05 266
Products Sold
Battery Product Part Number: 3200497-000 Battery lot codes: prior to 0539; lot codes: 05 265 or 05 266
Medtronic Emergency Response Systems, Inc. is recalling Batteries used with the LIFEPAK 20 defibrillator/monitor due to Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while op. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Defibrillator internal battery cell may contain a short which could reduce battery capacity and cause the device to shut down without warning while operating on backup (DC) battery power.
Recommended Action
Per FDA guidance
Firm sent letters on 03/30/2007 dated 03/2007 via certified return receipt to consignees with affected LIFEPAK 20 devices. The firm advised consignees to use the Operator's Checklist in the Operating Instructions to perform daily user tests and function checks while operating the defibrillator on battery power. In addition consignees are advised to replace their battery every 1 to 2 years.
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 noticeDistribution
As reported by FDA
IN
Page updated: Jan 10, 2026