FDA Device recall Z-0891-2021
Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-r…
- FDA Device
- Class II
- terminated
- Published 2021-02-03
On 2021-02-03 the FDA classified a Class II recall of Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-r… by Respironics California, citing ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended peri….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0891-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-10-30 |
| Published | 2021-02-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Respironics California |
| Distribution | US |
Product
Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Reason
Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
Identifiers
| code_info | Model: V60 Ventilator, Part Number 1076709 V60 Ventilator, JAPAN OPT: CFLEX,AVAPS,AT+ Serial Numbers: 100058561 1…Model: V60 Ventilator, Part Number 1076709 V60 Ventilator, JAPAN OPT: CFLEX,AVAPS,AT+ Serial Numbers: 100058561 100058562 100058565 100058572 100058573 100058574 100058576 100058835 100058840 100058844 100058845 100058846 100058902 100058903 100058904 100058905 100058906 100058908 100058911 100058914 100058917 100058968 100058970 100058971 100058975 100058977 100058990 100058991 100058994 100058997 100058999 100059002 100059149 100059153 100059163 100059239 100059248 100060123 100060124 100060214 100060215 100060216 100060219 100060220 100060222 100060229 100060232 100060234 100060236 100060239 100060328 100060329 100060330 100060331 100060339 100060340 100060341 100060344 100060345 100060346 100060347 100060388 100060389 100060398 100060400 100060402 100060404 100060406 100060407 100060409 100060410 100060416 100060476 100060483 100060484 100060486 100060487 100060488 100060490 100060491 100060492 10 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0891-2021%22
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