Olympus Pleuravideoscope — Class II medical device recall Z-1762-2020
Terminated recall by Olympus Corporation of the Americas, reported 2020-04-29, distributed nationwide. There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravide
| Recall number | Z-1762-2020 |
|---|---|
| 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 | 2020-03-23 |
| Classified | 2020-04-22 |
| Reported by FDA | 2020-04-29 |
| Terminated | 2021-11-30 |
| Distributed | Nationwide (US) |
| Quantity | 265 total |
| Model numbers | LTF-160 |
Product
Olympus Pleuravideoscope, Model LTF-160
Reason for recall
There was no data to validate that the identified endo-therapy devices were compatible with certain pleuravideoscope models. Updated Operations Manuals are being provided.
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-1762-2020. 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.