Philips Respironics V60 Ventilator — Class I medical device recall Z-0907-2022

Ongoing recall by Respironics California, LLC, reported 2022-04-27, distributed nationwide. Ventilator units have an issue impacting an internal electrical circuit within the ventilators, that in some c

Recall number	`Z-0907-2022`
Product type	Medical device
Classification	Class I
Status	Ongoing
Voluntary or mandated	Voluntary
Recalling firm	Respironics California, LLC, Carlsbad, CA, United States
Recall initiated	2022-02-28
Classified	2022-04-18
Reported by FDA	2022-04-27
Distributed	Nationwide (US)
Countries outside the US	AF, AR, AT, AU, BD, BE, BG, BH, BO, BR, CA, CH, CL, CN, CO, CY, CZ, DE, DK, DZ, EC, EG, ES, FI, FR, GB, GH, GR, GT, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KE, KR, KW, LB, LU, LV, MA, MT, MX, MY, NG, NL, NO, NP, NZ, OM, PA, PE, PH, PK, PL, PT, PY, QA, RO, SA, SE, SG, SI, TH, TR, TW, UA, VE, VN, ZA
Quantity	87,138 units
UPC / GTIN / UDI-DI	`00884838009844`, `00884838009851`, `00884838020054`, `00884838025776`, `00884838089280`, `00884838090996`
Serial numbers	`V60`

Product

Philips Respironics V60 Ventilator (All Models, including: 1053613, 1053614, 1053615, 1053616, 1053617, 1053618, 1076709, 1076716, 1076717, 1137292, DU1053617, U1053617, R1053618, R1076709)

Reason for recall

Ventilator units have an issue impacting an internal electrical circuit within the ventilators, that in some cases could result in the ventilator ceasing to operate.

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-0907-2022. 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.