FDA Device recall Z-1076-2018
GENICON EZEE Retrieval, sterile, Rx only
- FDA Device
- Class II
- terminated
- Published 2018-03-28
On 2018-03-28 the FDA classified a Class II recall of GENICON EZEE Retrieval, sterile, Rx only by Genicon, citing plastic handle is breaking off of shaft inhibiting proper removal per Instructions for Use.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1076-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-19 |
| Published | 2018-03-28 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Genicon |
| Distribution | FL, IL, MI, TN, UT |
Product
GENICON EZEE Retrieval, sterile, Rx only.
Reason
Plastic handle is breaking off of shaft inhibiting proper removal per Instructions for Use.
Identifiers
| code_info | Catalog No. 550-000-000; Lot No. I8095/2017-11-08, I8162-2018-01-09, I8162/2020-01-09; UDI: 00877972005223. |
|---|
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-1076-2018%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.