FDA Device recall Z-0902-2021
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-r…
- FDA Device
- Class II
- ongoing
- Published 2021-02-03
On 2021-02-03 the FDA classified a Class II recall of Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-r… by Respironics California, citing potential issues with ventilator navigation ring interface and liquid ingress: 1) The navigation ring may become inoperative or operate intermittently; 2) The navigation ring may….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0902-2021 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-11-02 |
| Published | 2021-02-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Respironics California |
| Distribution | US |
Product
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Reason
Potential issues with ventilator navigation ring interface and liquid ingress: 1) The navigation ring may become inoperative or operate intermittently; 2) The navigation ring may cause ventilator parameter values to change erratically during setting entries and adjustments.
Identifiers
| code_info | Model: V60 Part Number 1053613 V60 Ventilator,Intl Opt: CFLEX,AVAPS,PP Serial numbers: 100029460 100086827 100106522 1…Model: V60 Part Number 1053613 V60 Ventilator,Intl Opt: CFLEX,AVAPS,PP Serial numbers: 100029460 100086827 100106522 100125955 100173096 100173294 100173478 100173526 100173591 100173593 100173595 100174299 100174305 100174308 100190730 100252781 100252782 100252785 100304095 100304097 100304263 100304264 100304446 100304447 100304448 100304451 100304462 201022963 100190253 201024196 201025984 201025987 201025988 100176847 100176856 100252776 100315180 100315377 100315598 100315602 100315607 100315610 100315889 100350701 100361426 100363749 100370895 100375246 100044066 100074200 100074206 100074207 100085241 100085243 100085327 100102145 100102150 100102152 100102155 100114031 100118553 100118676 100118684 100119491 100120774 100138585 100138589 100146847 100146849 100147395 201008175 201008180 201008192 201008218 201008225 201008226 201013645 201013649 201013650 201014018 201014041 201014042 201014047 201031153 201031164 201031195 201031200 201031214 201031215 201031218 100039855 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: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0902-2021%22
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