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,

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.

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.