FDA Device recall Z-1660-2014
LIFEPAK 1000 defibrillator
- FDA Device
- Class II
- terminated
- Published 2014-06-04
On 2014-06-04 the FDA classified a Class II recall of LIFEPAK 1000 defibrillator by Physio Control, citing physio-Control has become aware of incidents where customers have attempted to use their LIFEPAK 1000 defibrillator and the device has shut down unexpectedly due to a very low bat….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1660-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-05-09 |
| Published | 2014-06-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Physio Control |
| Distribution | US |
Product
LIFEPAK 1000 defibrillator. Affected Part Numbers: 320371500XXX The LP1000 (in AED mode) is indicated for use on patients in cardiac arrest.
Reason
Physio-Control has become aware of incidents where customers have attempted to use their LIFEPAK 1000 defibrillator and the device has shut down unexpectedly due to a very low battery. A defibrillator in this scenario has the potential to fail to deliver a shock, with the potential result that therapy is not delivered and a patient is not resuscitated. A software malfunction in the LIFEPAK 100
Identifiers
| code_info | Affected Part Numbers: 320371500XXX *****SERIAL NUMBERS FOR US DEPARMENT OF DEFENSE****** 34876034 34876038 348…Affected Part Numbers: 320371500XXX *****SERIAL NUMBERS FOR US DEPARMENT OF DEFENSE****** 34876034 34876038 34876056 34876064 34876065 34877573 34877574 34877575 34877576 34877578 34877582 34988650 34988651 35122139 35147830 35215123 35215124 35908182 35908183 35972621 35972622 35972623 35972624 35972625 36059654 36065891 36065892 36065893 36065894 36065895 36065896 36065897 36065898 36066291 36066292 36066322 36066323 36066326 36066330 36066331 36066332 36066530 36066569 36066571 36066575 36066676 36085125 36089293 36089294 36089295 36089297 36103234 36103235 36103236 36103237 36103238 36103239 36103240 36103241 36103242 36103243 36103244 36103245 36103246 36103247 36103248 36103249 36103250 36103251 36103252 36103253 36103254 36103255 36103256 36103257 36134589 36145614 36153198 36153199 36153943 36156907 36217327 36217328 36217329 36217330 36217331 36217332 36217333 36217334 36217335 3621 |
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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-1660-2014%22
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