Biphasic LIFEPAK 15 Monitor/Defibrillator. Manufactured by Physio-Control Inc., a division of Medtronic, Inc. Redmond, Washington USA. The LIFEPAK 15 monitor/defibrillator is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient protocols.
FDA Recall Z-1410-2010 · Posted 2010-04-21
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Recalling FirmPhysio Control, Inc.
Recall StatusTerminated
Product CodeMKJ
Date Initiated2010-03-04
Date Terminated2012-01-03
Product Quantity3,609
Reason for Recall
Potential for the device to power off then on by itself, or to power off by itself and requiring the operator to turn it back on, or the device doesn't turn off.
Firm Action
Physio-Control Inc. issued an "Urgent Medical Device Correction" notification dated March 2010 to domestic consignees. Foreign consignees were notified by overseas representatives. Consignees were advised to keep the affected device in service and to test the units in accordance with operating instructions. They were further advised that a local service representative will call and schedule a service visit within 60 days. Consignees were asked to forward the notification to all of their sites and to notify the recalling firm if they no longer own the device.
For further information, contact Physio-Control Inc. Technical Support at 1-800-442-1142, Option 5, 6:00 am to 4:00 pm (Pacific), Monday-Friday.
Root Cause
Device Design
Distribution Pattern
Worldwide Distribution -- United States, Netherlands, Germany, Canada, Australia, and Hong Kong.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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