Class II

Medical Device Recall: Radial Jaw 4 Jumbo Biopsy Forceps with the following descriptions and UPN: Radial Jaw 4 Jumbo 240cm Box 5; Outer Box UPN: M00513363; Inner Box UPN: M00513360.

Boston Scientific Corporation · June 30, 2026

Reason for Recall

Potential for breach in sterile barrier of device packaging.

Distribution

US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KY, MA, MD, ME, MN, MO, MS, MT, NC, NJ, NM, NY, OH, PA, PR, SC, TN, TX, UT, VA, VT, WA, WI and International distribution pending.

States Affected

NATIONWIDE

Quantity Affected

5,020 (US); 20,770 (OUS)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2840-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.