Due to increased in complaints their is the potential for endoscopic clipping device to malfunction.
Reason for recall: Due to increased in complaints their is the potential for endoscopic clipping device to malfunction. 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, Quantity: 713,702 units Lot/code info: All Lots manufactured between 9/2/2023-04/20/2025 ; UDI: (01)10827002580104
10827002580104
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.