Recall Z-0304-2024— Physio-Control, Inc.
Class II · Ongoing
Class II FDA medical device recall by Physio-Control, Inc., initiated 2023-09-29. FDA's recall record names no specific 510(k) clearance for this event. Product: LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023. Reason: Their is a potential for battery pins to become loose within the defibrillator resulting in power issues..
- Recalling firm
- Physio-Control, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-09-29
- Firm location
- Redmond, WA, United States
Product description
LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023
Reason for recall
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
Data sourced from openFDA. This site is unofficial and independent of the FDA.