Wilson-Cook Medical Inc. recalls Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only

Recalling company

Wilson-Cook Medical Inc.

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Mar 3, 2026

Reported

Apr 22, 2026

Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and the countries of Argentina, AUSTRALIA, AUSTRIA, BAHRAIN, BELGIUM, Brunei, Darussalam, Brazil, Canada, CANARY ISLANDS, Chile, China, Colombia, Costa Rica, CROATIA, CYPRUS, CZECH REPUBLIC, DENMARK, Egypt, FINLAND, FRANCE, GERMANY, GREECE, Guatemala, Hong Kong, HUNGARY, Indonesia, India, IRELAND, ISRAEL, ITALIA, KUWAIT, LEBANON, LUXEMBOURG, MALTA, MAYOTTE, Mexico, Macao, MOROCCO, Malaysia, NEDERLAND, NORWAY, New Zealand, OMAN, PAKISTAN, Peru, POLAND, PORTUGAL, QATAR, REUNION, ROMANIA, SAUDI ARABIA, SLOVENIA, El Salvador, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, Thailand, TURKEY, Taiwan, United Arab Emirates, United Kingdom.

Status

Ongoing

Quantity

713,702 units

Lot / codes

All Lots manufactured between 9/2/2023-04/20/2025 ; UDI: (01)10827002580104

Company location

Winston Salem, NC

Recall type

Voluntary: Firm initiated

Recall number

Z-1812-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1812-2026 in the FDA Enforcement Report. Also see FDA recall press releases.