Medical Device Recall: BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Becton Dickinson & Company · October 14, 2025
Reason for Recall
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
Distribution
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.
States Affected
NATIONWIDE
Quantity Affected
4180000 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0504-2026
Status: ongoing
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