FDA Device recall Z-1687-2017
Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ventilator,Intl Opt: CFLEX,AVAPS,PPV V60 Ventilator,Intl Opt: CFLEX,AV…
- FDA Device
- Class II
- terminated
- Published 2017-04-05
On 2017-04-05 the FDA classified a Class II recall of Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ventilator,Intl Opt: CFLEX,AVAPS,PPV V60 Ventilator,Intl Opt: CFLEX,AV… by Respironics California, citing the V60 Ventilator with Version 2.20 software installed may falsely detect that the blower motor has stalled. If this condition occurs, the software will cause the ventilator to s….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1687-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-01 |
| Published | 2017-04-05 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Respironics California |
| Distribution | n/a |
Product
Philips V60 Ventilator with Version 2.20 Software, Description: V 60 Ventilator,Intl Opt: CFLEX,AVAPS,PPV V60 Ventilator,Intl Opt: CFLEX,AVAPS V60 Ventilator,Intl Opt: None V60 Ventilator,English Opt: None V60 Ventilator,Engl Opt: CFLEX,AVAPS V60 Us Demo Unit V60 USED ENGL OPT:CFLEX, AVAPS,PPV,AT+cl V60 VENT, JAPAN OPT: CFLEX, AVAPS, AT+ V60 VENT, JAPAN OPT: CFLEX, AVAPS, AT+ Catalog/REF No. 1053613, 1053614, 1053615, 1053616, 1053617, DU1053617, U1053617, 1076709, R1076709
Reason
The V60 Ventilator with Version 2.20 software installed may falsely detect that the blower motor has stalled. If this condition occurs, the software will cause the ventilator to shut down (Vent Inop) and display Error Code 100E. Ventilatory support will cease.
Identifiers
| code_info | Serial Number 100190253 100195884 201023008 201024196 201025984 201025987 201025988 201025947 201025972 20102…Serial Number 100190253 100195884 201023008 201024196 201025984 201025987 201025988 201025947 201025972 201025996 201026002 201023858 201026449 201026531 201026645 201026658 201026668 201025266 201026252 201026254 201026431 201026433 201026434 201026435 201026436 201026439 201026569 201026577 201026579 201026598 201026601 201026605 201026636 201026639 201026640 201026642 201026646 201026649 201026651 201026652 201026653 201026655 201026659 201026662 201026665 201026667 201026672 201026673 201026680 201026685 201026686 201026687 201026689 201026690 201026691 201026692 201026693 201026694 201026695 201026699 201026700 201026701 201026702 201026705 201026706 201026708 201026709 201026710 201026711 201026712 201026715 201026716 201026717 201026741 201026742 201026744 201026748 201026749 201026753 201026755 201026765 201026782 201024190 201026534 201025309 201025864 201025994 201026438 201024086 201025 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1687-2017%22
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