Philips Respironics V60 Ventilator Part Number DU1053617 — Class II medical device recall Z-0899-2021
Terminated recall by Respironics California, LLC, reported 2021-02-03, distributed nationwide. Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to o
| Recall number | Z-0899-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Respironics California, LLC, Carlsbad, CA, United States |
| Recall initiated | 2020-10-30 |
| Classified | 2021-01-22 |
| Reported by FDA | 2021-02-03 |
| Terminated | 2024-09-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, 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, IR, IS, IT, JO, JP, KE, KR, 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 | 481 systems |
| Serial numbers | 100002908, 100002911, 100002913, 100002914, 100002916, 100002959, 100003001, 100003003, 100003005, 100003007, 100003018, 100003046, 100003052, 100003081, 100003674, 100003675, 100003685, 100003689, 100003728, 100003736, 100003757, 100003909, 100003910, 100003913, 100003916 and 456 more |
| Model numbers | DU1053617, V60 |
Product
Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Reason for recall
Ventilator may experience potential issues with the backup battery failures: 1) if the battery is allowed to over discharge, or 2) if the ventilator is stored for an extended period of time without being plugged into AC power.
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-0899-2021. 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.