FDA Device recall Z-0817-2020
LIFEPAK 15 MONITOR/DEFIBRILLATOR service kits
- 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 service kits 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-0817-2020 |
| 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 service kits
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: 39432283 39432694 39432696 39432697 39432698 39432699 39432700 39432701 39432702 39432719 39…Serial numbers: 39432283 39432694 39432696 39432697 39432698 39432699 39432700 39432701 39432702 39432719 39432854 39432855 39432856 39432857 39432858 39432859 39432860 39432862 39432863 39432864 39432865 39432866 39432867 39432868 39432869 39432870 39432871 39432872 39432873 39432874 39432875 39432876 39432877 39432878 39432879 39432881 39432882 39432883 39432884 39432885 39432887 39432888 39432889 39432890 39432893 39432896 39432897 39432898 39432899 39432900 39432901 39435315 39436589 39451160 39451161 39451164 39451165 39451166 39451167 39451168 39451169 39451170 39451172 39451174 39451175 39451180 39451181 39451182 39451183 39451184 39451185 39451186 39451187 39451188 39451189 39451190 39451191 39451192 39451193 39451196 39451197 39451198 39451199 39451200 39451201 39451202 39451204 39451205 39451206 39451207 39451208 39451209 39451210 39451212 39451213 39451214 39451215 39451216 394 |
|---|
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-0817-2020%22
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