FDA Device recall Z-2818-2015
EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180
- FDA Device
- Class II
- terminated
- Published 2015-10-07
On 2015-10-07 the FDA classified a Class II recall of EVIS EXERA II Gastrovideoscope OLYMPUS GF type UCT180 by Olympus, citing insufficient information for specific cleaning accessories used for the cleaning and reprocessing of the GF-UCT180 ultrasound endoscope.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2818-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-21 |
| Published | 2015-10-07 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Olympus |
| Distribution | US |
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
Insufficient information for specific cleaning accessories used for the cleaning and reprocessing of the GF-UCT180 ultrasound endoscope
Identifiers
| code_info | Models: GF-UCT180 with serial numbers: 1110499 1210800 7410282 1310997 1311003 1311004 1310999 1311000 121057…Models: GF-UCT180 with serial numbers: 1110499 1210800 7410282 1310997 1311003 1311004 1310999 1311000 1210572 7310007 7310012 1210883 1310886 7510736 7510753 1110488 1110309 7410481 7410477 7310025 7510647 7510648 7510811 7510810 7510809 7510832 7510830 7510827 7510704 7410530 7410524 7410526 7410525 7510734 7510726 7510688 1210542 7410289 1311015 1311016 7410335 1210874 7410426 1210687 7410546 7410145 7310031 1110477 1110479 1110497 1310945 1110511 1110482 7510569 7410353 1110397 1100203 1100198 1110457 1110504 7310026 1110500 7410206 7510766 1311022 1110503 1210836 1210876 1210748 7510560 7510561 7410285 1210632 1210644 7510654 7510730 7510678 1210692 1210695 1210643 7510724 7510725 1310991 7510731 1310944 7310055 7310059 1110374 1110509 7310039 7510798 7410230 1210611 1210615 1210617 1210610 1210612 1210604 1210602 7410173 7410171 7410168 7410167 7410165 1210737 1210733 13111 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2818-2015%22
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