ENF-GP2 Rhino-Laryngo Fiberscope — Class II medical device recall Z-2292-2020
Terminated recall by Olympus Corporation of the Americas, reported 2020-06-17, distributed nationwide. Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with th
| Recall number | Z-2292-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Olympus Corporation of the Americas, Center Valley, PA, United States |
| Recall initiated | 2020-05-05 |
| Classified | 2020-06-08 |
| Reported by FDA | 2020-06-17 |
| Terminated | 2020-09-18 |
| Distributed | Nationwide (US) |
| Quantity | 19 |
| Serial numbers | 2801007, 2801008, 2801009, 2801010, 2801012, 2801019, 2801023, 2801046, 2801051, 2801058, 2801059, 2801069, 2801072, 2801076, 2901130, 2901343, 2901410, 2901414, 2901428, 2901435, 2901437, 2901451, 2901456, 2901529, 2901548 and 22 more |
Product
ENF-GP2 Rhino-Laryngo Fiberscope - Product Usage: is indicated for use within the nasal and nasopharyngeal lumen.
Reason for recall
Products repaired with the incorrect service manual may be missing an O ring and are subject to rework with the corrected service manual.
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-2292-2020. 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.