FDA Device recall Z-1812-2026
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
- FDA Device
- Class II
- ongoing
- Published 2026-04-22
On 2026-04-22 the FDA classified a Class II recall of Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO by Wilson Cook Medical, citing due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1812-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-03-03 |
| Published | 2026-04-22 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Wilson Cook Medical |
| Distribution | US |
Product
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Reason
Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Identifiers
| code_info | All Lots manufactured between 9/2/2023-04/20/2025 ; UDI: (01)10827002580104 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
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All Wilson Cook Medical recalls
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1812-2026%22
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