Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1812-2026 — Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

U.S. FDA — Device Enforcement · United States · 2026-03-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1812-2026
Date of alert
2026-03-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Wilson-Cook Medical Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10827002580104
Reported risk: Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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