EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 — Class II medical device recall Z-2818-2015
Terminated recall by Olympus Corporation of the Americas, reported 2015-10-07, distributed nationwide. Insufficient information for specific cleaning accessories used for the cleaning and reprocessing of the GF-UC
| Recall number | Z-2818-2015 |
|---|---|
| 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 | 2015-08-21 |
| Classified | 2015-09-28 |
| Reported by FDA | 2015-10-07 |
| Terminated | 2017-05-08 |
| Distributed | Nationwide (US) |
| Quantity | 1,014 |
| Serial numbers | 1000109, 1000130, 1000131, 1000133, 1000137, 1000142, 1000144, 1000149, 1000152, 1000155, 1000156, 1000157, 1000160, 1000162, 1000163, 1000164, 1000165, 1000166, 1000169, 1000171, 1000173, 1000174, 1100175, 1100176, 1100189 and 475 more |
| Model numbers | GF-UCT180 |
Product
EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180; designed for endoscopic real-time ultrasound imaging, ultrasound guided needle aspiration and other endoscopic procedures within the upper gastrointestinal tract and surrounding organs.
Reason for recall
Insufficient information for specific cleaning accessories used for the cleaning and reprocessing of the GF-UCT180 ultrasound endoscope
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-2818-2015. 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.