FDA Device recall Z-0894-2021
Philips Respironics V60 Ventilator Part Number 1076716 - 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 1076716 - 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-0894-2021 |
| 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 1076716 - 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 1076716 V60 Ventilator, CHINA OPT: CFLEX, AVAPS Serial Numbers: 100193935 1001…Model: V60 Ventilator, Part Number 1076716 V60 Ventilator, CHINA OPT: CFLEX, AVAPS Serial Numbers: 100193935 100194169 100030124 100030335 100030359 100030360 100030761 100030762 100030763 100030764 100030766 100030767 100030768 100030769 100030770 100030771 100030773 100030775 100030776 100030777 100030779 100030782 100030783 100030784 100032461 100032686 100032687 100032688 100032689 100032690 100032691 100032692 100032695 100032697 100032698 100032701 100032702 100035773 100035778 100035779 100035896 100035897 100035898 100035899 100035900 100035901 100035902 100035903 100035904 100035907 100035909 100035910 100035911 100035913 100035914 100035918 100035919 100035926 100036047 100036302 100036306 100036307 100036310 100036311 100036313 100036314 100036316 100036317 100036320 100036432 100036433 100036434 100036439 100037365 100037366 100037367 100037368 100037369 100037370 100037371 100037372 10003 |
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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-0894-2021%22
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