Recall Z-0504-2026— Becton Dickinson & Company
Class II · Ongoing
Class II FDA medical device recall by Becton Dickinson & Company, initiated 2025-10-14. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Becton Dickinson & Company
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-10-14
- Firm location
- Franklin Lakes, NJ, United States
Product description
BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Reason for recall
BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
Data sourced from openFDA. This site is unofficial and independent of the FDA.