Becton Dickinson & Company recalls BD Luer Tip Caps
- Recalling company
- Becton Dickinson & Company
- Product
- BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
- Reason
- BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 14, 2025
- Reported
- Nov 26, 2025
- 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.
- Status
- Ongoing
- Quantity
- 4180000 units
- Lot / codes
- Catalog Number(s) or Model Number(s): 308341; UDI-DI: 50382903083416; Lot Numbers: 5029670, 5034211, 5041975;
- Company location
- Franklin Lakes, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0504-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0504-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.