BD 10mL Non-Sterile Syringe recalled for wrong Luer type in packaging
Becton Dickinson discovered that some Luer Slip syringes were accidentally mixed into batches of 10mL Luer-Lok syringes during packaging. This affects product Catalog Number 301029, Lot 5268614, distributed in California and Texas. No injuries have been reported.
From the FDA notice · Read the official notice ↗ · All Becton Dickinson recalls
What to do
- Check if you have BD 10mL syringes (Catalog 301029) with Lot Number 5268614 and expiration date 08/31/2030
- Verify the syringe tip type matches your needs (Luer-Lok vs. Luer Slip)
- Contact your supplier or Becton Dickinson if you have affected product for guidance on replacement or return
Is yours affected?
Compare your label or packaging with the recalled product.
- Product
- 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
- Sold in
- Nationwide
- Made for
- All ages (0 months and older)
Details
- Units affected
- 204,000 units
- Illnesses reported
- None reported
- Manufactured in
- 1 Becton Dr, N/A, Franklin Lakes, NJ, United States
- Classification
- Class II
- Recall number
- Z-1496-2026
In the FDA's words
- Description
- 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case. During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. Catalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030. Distribution: US Nationwide distribution in the states of California and Texas. Affected quantity: 204,000 units
- Hazard
- During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.