Becton Dickinson & Company recalls BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;

Recall date

October 14, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0504-2026

FDA classification

Class II

Brand / firm

Becton Dickinson & Company

Sold / distributed

Worldwide - US Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WV and the countries of Canada, Singapore, Hong Kong.

Why it was recalled

BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;