Philips Trilogy 100 Ventilator — Class I medical device recall Z-0882-2023
Ongoing recall by Philips Respironics, Inc., reported 2023-01-18, distributed nationwide. The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may sepa
| Recall number | Z-0882-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Respironics, Inc., Murrysville, PA, United States |
| Recall initiated | 2022-12-07 |
| Classified | 2023-01-06 |
| Reported by FDA | 2023-01-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, BR, CA, CN, DE, JP, KR |
| Quantity | 20,807 |
| UPC / GTIN / UDI-DI | 00606959023178, 00606959034020, 00606959034037, 00606959429048, 00606959429055, 00606959429079, 00606959429086, 00606959429093, 00606959429116, 00606959429130, 00606959429246, 00606959429253, 00606959429314, 00606959429321, 00606959429383, 00606959429413, 00606959429420, 00606959429482, 00606959429499, 00606959429536, 00606959429628, 00606959429635, 00606959429680, 00606959429697 |
| Serial numbers | TV109061712, TV109061803, TV109071304, TV109072104, TV109081223, TV109090828, TV109090934, TV109091114, TV109091121, TV109091412, TV109091418, TV109092109, TV109101937, TV109102213, TV109102247, TV109102251, TV109102602, TV109102631, TV109111424, TV109111810, TV109111825, TV109111834, TV109111918, TV109121209, TV109121406 and 475 more |
| Model numbers | 1054096, 1054096B, 1054097, 1054260, 1054260B, 1054655, 1054655B, 1054655TP, 1054655TPV, AU1054096, AU1054096B, BR1054096, BT1054260, CA1054096, CA1054096B, CN1054096, KO1054096, KR1054096, LA1054096, R1054260, R1054260B, R1054655B, R1054655TP, R1054655TPV, RSL1054260 and 2 more |
Product
Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B, R1054260, RSL1054260, CA1054096, R1054260B, R1054655TPV, AU1054096, AU1054096B, 1054096B, 1054097, BR1054096, LA1054096, CN1054096, KO1054096, KR1054096, R1054655TP, R1054655B, 1054655, 1054655TPV, 1054655TP, 1054655B
Reason for recall
The replacement silicone sound abatement foam installed into some Trilogy 100 and Trilogy 200 devices may separate from the plastic backing to which it is attached. If this were to happen, the foam could potentially block air inlet, which could result in a reduction in delivered therapy volume or pressure and could cause the device to alarm.
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-0882-2023. 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.