FDA Device recall Z-0816-2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad
- FDA Device
- Class II
- terminated
- Published 2020-01-22
On 2020-01-22 the FDA classified a Class II recall of LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad by Physio Control, citing monitor/Defibrillator may not deliver a shock after the "Shock" button on the keypad is pressed as a result of oxidation that has formed over time within the button.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0816-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-20 |
| Published | 2020-01-22 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Physio Control |
| Distribution | US |
Product
LIFEPAK 15 MONITOR/DEFIBRILLATOR that was either manufactured with or received an upgrade kit that contained an affected keypad.
Reason
Monitor/Defibrillator may not deliver a shock after the "Shock" button on the keypad is pressed as a result of oxidation that has formed over time within the button.
Identifiers
| code_info | Serial numbers: 37964613 37964617 37964621 37964628 37964630 37968424 37968429 37964596 37964601 37964607 37…Serial numbers: 37964613 37964617 37964621 37964628 37964630 37968424 37968429 37964596 37964601 37964607 37964610 37968715 37968716 37968717 37968718 37968721 37968722 37968724 38046540 38046549 38046552 38046565 38046571 38046572 38046573 38051949 38051951 38051954 38051955 38051958 38051963 38051969 38051972 38051973 38051974 38051980 38053216 38053218 38053220 38053221 38053225 38053231 38053233 38053236 38053239 38059568 38059570 38059574 38059591 38120769 38120772 38120775 38120780 38120781 38120783 38120784 38120787 38120788 38120790 38124016 38124030 38124035 38124042 38124044 38124047 38125969 38125971 38125972 38125980 38125982 38125987 38125990 38126255 38126258 38126260 38126265 38126267 38126269 38126272 38126273 38126277 38127130 38127131 38127132 38127134 38127136 38127138 38127139 38127140 38127141 38127143 38127144 38130272 38130273 38130276 38130277 38130279 38130282 381 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0816-2020%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.