FDA Device recall Z-1144-2017

LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option

FDA Device
Class II
terminated
Published 2017-02-15

On 2017-02-15 the FDA classified a Class II recall of LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option by Physio Control, citing the End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX after start-up or during device operation.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1144-2017
Classification	Class II
Status	terminated
Initiated	2017-01-16
Published	2017-02-15
Last updated	2026-09-13 11:54 UTC
Company	Physio Control
Distribution	US

Product

LIFEPAK 15 Monitor/Defibrillator with End-Tidal CO2 option. Intended for use by trained medical personnel in out-of-doors and indoor emergency care settings within the environmental conditions specified in the Operating Instructions.

Reason

The End-Tidal CO2 (EtCO2) reading can intermittently show a value of XXX after start-up or during device operation.

Identifiers

code_info	LOT NUMBERS OF AFFECTED MODULE: Lot # 1506, 1520, 1532, 1544, and 1551. SERIAL NUMBERS OF AFFECTED DEVICES:… LOT NUMBERS OF AFFECTED MODULE: Lot # 1506, 1520, 1532, 1544, and 1551. SERIAL NUMBERS OF AFFECTED DEVICES: 37930990, 38046566, 38130282, 38200467, 38374121, 38544771, 38561025, 38567823, 38577667, 38763423, 38805573, 39229417, 39656903, 39749477, 39757723, 39757723, 39905189, 40007558, 40007616, 40008237, 40074226, 40246186, 40637428, 40639397, 40881488, 41119327, 41441205, 41734558, 41908077, 42036185, 42721982, 42759819, 43273957, 43981182, 44128955, 44143195, 44143356, 44143399, 44143438, 44143481, 44143616, 44143674, 44143708, 44143786, 44143811, 44143814, 44143891, 44143894, 44143984, 44146278, 44146304, 44146408, 44148345, 44148588, 44148641, 44150897, 44151007, 44151084, 44151151, 44151156, 44151224, 44151362, 44151498, 44151591, 44151697, 44151790, 44151809, 44151862, 44151920, 44151995, 44152133, 44152249, 44152345, 44152361, 44156527, 44157048, 44157124, 44157189, 44157404, 44157697, 44157711, 44158485, 44158543, 44158614, 44158707, 44158804, 44159096, 44159162, 4

code_info

LOT NUMBERS OF AFFECTED MODULE: Lot # 1506, 1520, 1532, 1544, and 1551. SERIAL NUMBERS OF AFFECTED DEVICES:…

LOT NUMBERS OF AFFECTED MODULE: Lot # 1506, 1520, 1532, 1544, and 1551. SERIAL NUMBERS OF AFFECTED DEVICES: 37930990, 38046566, 38130282, 38200467, 38374121, 38544771, 38561025, 38567823, 38577667, 38763423, 38805573, 39229417, 39656903, 39749477, 39757723, 39757723, 39905189, 40007558, 40007616, 40008237, 40074226, 40246186, 40637428, 40639397, 40881488, 41119327, 41441205, 41734558, 41908077, 42036185, 42721982, 42759819, 43273957, 43981182, 44128955, 44143195, 44143356, 44143399, 44143438, 44143481, 44143616, 44143674, 44143708, 44143786, 44143811, 44143814, 44143891, 44143894, 44143984, 44146278, 44146304, 44146408, 44148345, 44148588, 44148641, 44150897, 44151007, 44151084, 44151151, 44151156, 44151224, 44151362, 44151498, 44151591, 44151697, 44151790, 44151809, 44151862, 44151920, 44151995, 44152133, 44152249, 44152345, 44152361, 44156527, 44157048, 44157124, 44157189, 44157404, 44157697, 44157711, 44158485, 44158543, 44158614, 44158707, 44158804, 44159096, 44159162, 4

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1144-2017%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.