TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP — Class II medical device recall Z-0557-2024
Ongoing recall by Olympus Corporation of the Americas, reported 2023-12-20, distributed nationwide. Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
| Recall number | Z-0557-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2023-09-28 |
| Classified | 2023-12-14 |
| Reported by FDA | 2023-12-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, JP |
| Quantity | 75 |
| UPC / GTIN / UDI-DI | 04953170061998, 04953170340215 |
| Serial numbers | 2018337, 2018435, 2018486, 2018543, 2018571, 2018675, 2319768, 2319820, 2510582, 2515143, 2515181, 2515449, 2515549, 2615760, 2615761, 2615763, 2615825, 2615830, 2615831, 2616057, 2616130, 2616199, 2621001, 2716417, 2817430 and 7 more |
Product
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Reason for recall
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
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-0557-2024. 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.