Philips Respironics V60 Plus Ventilator Part Number 1138747 — Class I medical device recall Z-0663-2022
Ongoing recall by Respironics California, LLC, reported 2022-03-09, distributed in AR, CA, FL, GA, IN, LA, MD, MO…. A limited number of ventilators were assembled with expired adhesive. If the adhesive fails, a bracket may bec
| Recall number | Z-0663-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Respironics California, LLC, Carlsbad, CA, United States |
| Recall initiated | 2022-01-24 |
| Classified | 2022-02-25 |
| Reported by FDA | 2022-03-09 |
| Distributed | AR, CA, FL, GA, IN, LA, MD, MO, NY, PA, SC, TN, TX |
| Quantity | 294 systems |
| UPC / GTIN / UDI-DI | 00884838090996 |
| Model numbers | 1138747, V60 |
Product
Philips Respironics V60 Plus Ventilator Part Number 1138747
Reason for recall
A limited number of ventilators were assembled with expired adhesive. If the adhesive fails, a bracket may become loose and potentially damage the capacitors, which could cause the ventilator to stop providing ventilation to the patient. This failure may either activate both visual and audible alarms, or it may not sound or display an alarm (a silent shutdown).
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-0663-2022. 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.