FDA Device recall Z-2276-2020
Genicon Natura Model 210-005-251, 5mm diameter, 150mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a…
- FDA Device
- Class II
- ongoing
- Published 2020-06-17
On 2020-06-17 the FDA classified a Class II recall of Genicon Natura Model 210-005-251, 5mm diameter, 150mm length (one cannula, threaded) - Product Usage: The universal handle can be used as a… 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-2276-2020 |
| 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 210-005-251, 5mm diameter, 150mm 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 | Lot I8880-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-2276-2020%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.