Becton Dickinson & Company recalls 10mL Non-Sterile BD Luer-Lok Tip Syringe Only.
- Recalling company
- Becton Dickinson & Company
- Product
- 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
- Reason
- During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Jan 27, 2026
- Reported
- Mar 18, 2026
- Distribution
- US Nationwide distribution in the states of California and Texas.
- Status
- Ongoing
- Quantity
- 204,000 units
- Lot / codes
- Catalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.
- Company location
- Franklin Lakes, NJ
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1496-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1496-2026 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.