FDA Device recall Z-1082-2013
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators
- FDA Device
- Class II
- terminated
- Published 2013-04-17
On 2013-04-17 the FDA classified a Class II recall of The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators by Physio Control, citing LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1082-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-02-08 |
| Published | 2013-04-17 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Physio Control |
| Distribution | n/a |
Product
The LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators. Product part's numbers: 3200731-xxx, 3202177-xxx, U3200731-xxx, and U3202177-006. Automated external defibrillators.
Reason
LIFEPAK CR Plus or LIFEPAK Express Automated External Defibrillators (AEDs) are recalled due to the potential to experience an early internal battery depletion issue.
Identifiers
| code_info | Serial numbers of devices distributed in the US: 33219251, 33220310, 33220344, 33220367, 33220369, 33220376, 33220402,…Serial numbers of devices distributed in the US: 33219251, 33220310, 33220344, 33220367, 33220369, 33220376, 33220402, 33220450, 33220461, 33220464, 33220466, 33220470, 33221200, 33221394, 33231481, 33231486, 33231488, 33231492, 33231511, 33231512, 33231521, 33231523, 33231524, 33231527, 33231532, 33231535, 33231536, 33231539, 33231545, 33231546, 33231554, 33231611, 33231614, 33231618, 33231623, 33231625, 33231628, 33231635, 33231636, 33231639, 33231641, 33231685, 33231712, 33231728, 33231733, 33231737, 33231741, 33231745, 33231755, 33231758, 33232813, 33232814, 33232816, 33237363, 33238809, 33239104, 33239111, 33239118, 33239125, 33239127, 33239134, 33239139, 33239154, 33239159, 33239164, 33239184, 33239194, 33239206, 33239243, 33239251, 33239260, 33239261, 33239262, 33239264, 33239265, 33239267, 33240071, 33240074, 33240087, 33240093, 33240102, 33240104, 33240106, 33240109, 33243833, 33243849, 33243931, 33243932, 33246462, 33246464, 33246487, 33246497, 33246540, 33246541, 33246542, |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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FDA Device · Class II · 2025-09-10 · Physio Control - LIFEPAK 15 Part / Catalog Numbers / UDI-DI code: V15-7-000022 / 99577-001957 / 883873871690 V15-2-000051 / 99577-000046 / 883873988022 V15-…
FDA Device · Class II · 2025-09-10 · Physio Control - LIFEPAK 1000 Part / Catalog Numbers / UDI-DI code: 320371500023 / 99425-000025 / 885074698953 320371500229 / 99425-000025 / 885074698953 33…
FDA Device · Class II · 2025-09-10 · Physio Control
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1082-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.