FDA Device recall Z-0890-2021
Philips Respironics V60 Ventilator Part Number 1053618 - 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 1053618 - 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-0890-2021 |
| 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 1053618 - 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 1053618 V60 Ventilator, Japan Opt: CFLEX,AVAPS Serial Numbers: 100019618 10001…Model: V60 Ventilator, Part Number 1053618 V60 Ventilator, Japan Opt: CFLEX,AVAPS Serial Numbers: 100019618 100019631 100019639 100019822 100019823 100019824 100019827 100019838 100019917 100019920 100019922 100019924 100019965 100019966 100019967 100019971 100019972 100020663 100020664 100020665 100020666 100022148 100023892 100023893 100023894 100023896 100023897 100023899 100023905 100023909 100023940 100023941 100023944 100023956 100023995 100023998 100024000 100024003 100024007 100024008 100024688 100025546 100025549 100026087 100026088 100026089 100026090 100026092 100026095 100026124 100027090 100027095 100027100 100027101 100027108 100027114 100027174 100027176 100027181 100027185 100027191 100027199 100027200 100027543 100027546 100027547 100027548 100027550 100027552 100030134 100030201 100030203 100030205 100030206 100030211 100030355 100031913 100031917 100031921 100031937 100031941 100031 |
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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-0890-2021%22
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