Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II — Class II medical device recall Z-1929-2017
Terminated recall by Olympus Corporation of the Americas, reported 2017-05-10, distributed nationwide. A damaged temperature sensor at the endoscope's tip can cause the endoscope's distal end to become abnormally
| Recall number | Z-1929-2017 |
|---|---|
| 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 | 2017-02-10 |
| Classified | 2017-05-03 |
| Reported by FDA | 2017-05-10 |
| Terminated | 2018-05-09 |
| Distributed | Nationwide (US) |
| Quantity | 863 units |
| Model numbers | W7100603, WA50040A |
Product
Olympus ENDOEYE HD II Video Telescopes Models: WA50040A Endoeye HD II, 10 mm, 0 deg., autoclavable; WA50042A Endoeye HD II, 10 mm, 30 deg., autoclavable; repair cable 10mm 0/30 deg., part number W7100603
Reason for recall
A damaged temperature sensor at the endoscope's tip can cause the endoscope's distal end to become abnormally hot.
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-1929-2017. 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.