Recall
FDAHealthMarch 3, 2026

Wilson-Cook Medical Inc. — Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

⚠️ Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
March 3, 2026

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.

What's affected?

Product
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Lot code
manufactured

Additional details

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

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 713,702 units.

View original FDA notice →

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