Philips Respironics V60/V60 Plus Ventilator — Class I medical device recall Z-2631-2023
Ongoing recall by Philips Respironics, Inc., reported 2023-10-04, distributed in CA, OH, OR, SC. Power Management PCBAs may malfunction, causing a power failure leading to ventilator loss of function.
| Recall number | Z-2631-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Respironics, Inc., Murrysville, PA, United States |
| Recall initiated | 2023-08-25 |
| Classified | 2023-09-28 |
| Reported by FDA | 2023-10-04 |
| Distributed | CA, OH, OR, SC |
| Countries outside the US | PH |
| Reason classes | device malfunction |
| Serial numbers | 100006889, 100006900, 100013579, 100082334, 100085632, 100246411, 100246416, 100293267, 100423818, 201010175, 201014394, 201017048, 201019564, SC231104X, SC23110EV, SC23110MF, SC2311127, SC2311138, SC2311165, SC2311168, SC231116C, SC231117H, SC23120K8, SC23120NH, SC2312133 and 1 more |
| Model numbers | 1053617, 453561544461, V60 |
Product
Philips Respironics V60/V60 Plus Ventilator, PCBA Part Number: 453561544461 V60 Device Part Numbers 1053617 (US) and 1137276 (Philippines)
Reason for recall
Power Management PCBAs may malfunction, causing a power failure leading to ventilator loss of function.
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-2631-2023. 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.