FDA Device recall Z-0887-2021
Philips Respironics V60 Ventilator Part Number 1053615 - 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 1053615 - 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-0887-2021 |
| 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 1053615 - 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 1053615 V60 Ventilator, Intl Opt: NONE Serial Numbers: 100011125 100021457 10…Model: V60 Ventilator, Part Number 1053615 V60 Ventilator, Intl Opt: NONE Serial Numbers: 100011125 100021457 100049066 100049185 100049195 100049196 100049200 100122592 100172279 201003463 100011045 100013970 100013971 100015382 100097294 100106739 100109494 100109498 100109499 100109504 100110679 100120770 100036303 100036437 100036446 100036447 100036452 100120864 100085138 100101080 100160827 100006791 100006794 100006805 100007128 100007199 100007208 100007342 100010908 100011086 100011088 100011089 100011090 100011124 100011127 100011187 100013251 100013252 100013253 100013254 100013255 100013256 100013282 100013934 100014019 100014024 100014518 100015338 100015342 100015343 100015389 100015760 100016617 100016618 100016619 100016921 100016927 100016928 100016929 100017340 100017341 100017344 100017350 100017352 100017353 100019976 100020060 100020124 100020748 100020751 100020753 100020755 100 |
|---|
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-0887-2021%22
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