Philips V60 Ventilators — Class I medical device recall Z-2061-2017
Terminated recall by Respironics California Inc, reported 2017-05-24, distributed nationwide. Over time, low-frequency vibrations can cause the pins within the female connectors on the Motor Controller to
| Recall number | Z-2061-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Respironics California Inc, Carlsbad, CA, United States |
| Recall initiated | 2017-04-24 |
| Classified | 2017-05-17 |
| Reported by FDA | 2017-05-24 |
| Terminated | 2018-08-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BB, BE, BH, BO, BR, CA, CH, CL, CN, CO, CZ, DE, DK, DO, EC, EG, ES, FI, FR, GB, HK, HR, ID, IE, IL, IN, IR, IS, IT, JO, KE, KR, KW, LB, MA, MT, MX, MY, NG, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, PY, QA, RS, SA, SE, SG, SI, TH, TR, TW, VE, VN, ZA |
| Quantity | 30,516 units |
| UPC / GTIN / UDI-DI | 00989805616411, 00989805627431, 00989805636631 |
| Serial numbers | 100003256, 100003311, 100003563, 100004666, 100004675, 100004678, 100004680, 100004682, 100004748, 100004794, 100004925, 100005812, 100005814, 100005892, 100005902, 100005981, 100005983, 100005984, 100006103, 100006111, 100006113, 100006170, 100006172, 100006173, 100006174 and 475 more |
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2061-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.