Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic… — Class II medical device recall Z-2706-2017
Terminated recall by Fujifilm Medical Systems U.S.A., Inc., reported 2017-07-19, distributed in AL, HI, MO. Fujifilm is recalling multiple endoscopes after a retrospective review.
| Recall number | Z-2706-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fujifilm Medical Systems U.S.A., Inc., Wayne, NJ, United States |
| Recall initiated | 2017-02-17 |
| Classified | 2017-07-10 |
| Reported by FDA | 2017-07-19 |
| Terminated | 2018-10-03 |
| Distributed | AL, HI, MO |
| Quantity | 4 units |
| Model numbers | EG-530UTA |
Product
Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripheral organs
Reason for recall
Fujifilm is recalling multiple endoscopes after a retrospective review.
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-2706-2017. 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.