FDA Device recall Z-2706-2017
Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripher…
- FDA Device
- Class II
- terminated
- Published 2017-07-19
On 2017-07-19 the FDA classified a Class II recall of Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripher… by Fujifilm Medical Systems U, citing fujifilm is recalling multiple endoscopes after a retrospective review.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2706-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-17 |
| Published | 2017-07-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Fujifilm Medical Systems U |
| Distribution | AL, HI, MO |
Product
Ultrasonic Endoscope Model Number EG-530UT A flexible ultrasonic endoscope intended to provide ultrasonic images of submucosal and peripheral organs
Reason
Fujifilm is recalling multiple endoscopes after a retrospective review.
Identifiers
| code_info | 1U881A131 1U88A1A145 3U881A005 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2706-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.