FDA Device recall Z-0910-2021
Philips Respironics V60 Ventilator Part Number R1076709 - Product Usage: intended to be used only with various combinations of Respironics-…
- 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 R1076709 - Product Usage: intended to be used only with various combinations of Respironics-… 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-0910-2021 |
| 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 R1076709 - 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: R1076709 V60 Ventilator, JAPAN OPT: CFLEX,AVAPS,AT+ Serial Numbers: 100065352 100065365…Model: V60 Part Number: R1076709 V60 Ventilator, JAPAN OPT: CFLEX,AVAPS,AT+ Serial Numbers: 100065352 100065365 100065371 100065487 100065493 100067423 100067425 100067428 100067431 100067451 100068214 100069518 100070301 100070306 100070398 100070476 100070491 100070492 100070768 100070774 100070776 100070777 100070778 100070780 100070781 100070859 100070862 100070865 100070921 100070922 100070924 100070928 100070929 100070930 100070935 100070966 100070969 100070973 100070976 100070981 100071071 100071073 100071077 100071123 100071461 100071510 100071511 100072415 100072417 100072418 100072499 100072570 100072606 100072607 100072673 100072676 100072679 100072684 100072685 100072688 100072690 100072695 100074195 100075099 100075100 100075104 100075189 100075293 100075312 100075381 100078120 100078132 100078140 100078145 100078266 100078302 100078313 100078362 100078365 100078366 100078372 100079387 |
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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-0910-2021%22
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