Data Foundry

Medical device recalls 2017

Philips V60 Ventilator with Version 2 — Class II medical device recall Z-1687-2017

Terminated recall by Respironics California Inc, reported 2017-04-05. The V60 Ventilator with Version 2.20 software installed may falsely detect that the blower motor has stalled.

Recall numberZ-1687-2017
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmRespironics California Inc, Carlsbad, CA, United States
Recall initiated2017-02-01
Classified2017-03-27
Reported by FDA2017-04-05
Terminated2018-06-26
Countries outside the USAE, AR, AT, BE, CA, CH, CZ, DE, ES, FI, FR, GB, HK, ID, IN, IS, IT, JP, KW, MX, MY, NL, NO, QA, SA, SE, TR, VN
Quantity2,512 units
Reason classessoftware
Serial numbers100136136, 100136655, 100141903, 100146850, 100146852, 100149714, 100153310, 100158909, 100160567, 100160569, 100166344, 100172321, 100173878, 100189742, 100189753, 100189758, 100189759, 100190088, 100190090, 100190093, 100190095, 100190190, 100190253, 100190730, 100190731 and 475 more
Model numbers1053613, 1053614, 1053615, 1053616, 1053617, 1076709, DU1053617, R1076709, U1053617

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 for recall

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.

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-1687-2017. 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.