FDA Device recall Z-2274-2020
Genicon Natura Model 210-005-151
- FDA Device
- Class II
- ongoing
- Published 2020-06-17
On 2020-06-17 the FDA classified a Class II recall of Genicon Natura Model 210-005-151 by Genicon, citing there is potential for the plastic optical tip to become detached from the metal shaft.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2274-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-08-21 |
| Published | 2020-06-17 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Genicon |
| Distribution | AL, DE, FL, GA, MO, NC, TN |
Product
Genicon Natura Model 210-005-151; 5mm diameter, 100mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a pistol grip or like a traditional Trocar handle when using a scope.
Reason
There is potential for the plastic optical tip to become detached from the metal shaft.
Identifiers
| code_info | Lots I8081-A, I7914-A, and I8033-A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2274-2020%22
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