Becton Dickinson & Company: Device Recall
Recall #Z-0504-2026 · 10/14/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0504-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Becton Dickinson & Company
- Status
- Ongoing
- Date Initiated
- 10/14/2025
- Location
- Franklin Lakes, NJ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 4180000 units
Reason for Recall
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
Product Description
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Distribution Pattern
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.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.