FDA Device recall Z-2061-2017
Philips V60 Ventilators, Material No. 850008, 1053613, 1053614, 1053615, 1053616, 1053617, 1076715, 1076716, 1076717, DU1053617, U1053617
- FDA Device
- Class I
- terminated
- Published 2017-05-24
On 2017-05-24 the FDA classified a Class I recall of Philips V60 Ventilators, Material No. 850008, 1053613, 1053614, 1053615, 1053616, 1053617, 1076715, 1076716, 1076717, DU1053617, U1053617 by Respironics California, citing over time, low-frequency vibrations can cause the pins within the female connectors on the Motor Controller to Data Acquisition Board ribbon cable to become partially displaced ca….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2061-2017 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2017-04-24 |
| Published | 2017-05-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Respironics California |
| Distribution | US |
Product
Philips V60 Ventilators, Material No. 850008, 1053613, 1053614, 1053615, 1053616, 1053617, 1076715, 1076716, 1076717, DU1053617, U1053617. Old Material No. 850008, 989805628251, 989805612101, 989805613391, 989805613661, 989805611761, 989805627411, 989805627431, 989805627441, 989805616411, 989805636631.
Reason
Over time, low-frequency vibrations can cause the pins within the female connectors on the Motor Controller to Data Acquisition Board ribbon cable to become partially displaced causing momentary high resistance that prevents or restricts data travelling through the cable during the high resistance event.
Identifiers
| code_info | As-Shipped System Serial Number 100027294 100061625 100061627 100061638 100061640 100061641 100073201 100073243…As-Shipped System Serial Number 100027294 100061625 100061627 100061638 100061640 100061641 100073201 100073243 100073250 100073259 100084756 100120124 100120850 201003948 201009965 201009974 100003256 100003311 100004748 100005812 100005814 100005902 100005983 100006103 100006113 100006172 100006173 100006174 100006176 100006185 100007117 100007119 100007191 100007197 100007209 100007334 100007341 100007414 100007418 100007422 100007536 100007539 100007543 100007768 100007769 100007770 100007771 100007776 100007780 100007781 100007782 100007786 100007879 100007882 100007888 100010702 100010703 100010707 100010708 100010709 100010710 100010712 100010720 100010851 100010853 100010902 100010904 100010905 100010911 100011043 100011045 100013961 100013965 100013970 100013971 100014010 100014469 100014483 100014489 100014516 100014770 100014772 100014773 100014775 100014776 100014778 100014822 100014823 |
|---|
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-2061-2017%22
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