BD syringe batch may contain Luer Slip instead of Luer Lok
Becton Dickinson is recalling one lot of 10 mL Non-Sterile BD Luer-Lok Tip Syringes because some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Rubric level 2 covers low-risk, precautionary recalls: the fault is a product mix-up during packaging rather than a defect, and the source describes no hazard, illness or injury.
Plain-English summary
Becton Dickinson & Company is recalling the 10 mL Non-Sterile BD Luer-Lok Tip Syringe, catalogue number 301029, supplied 850 bulk non-sterile units per case. About 204,000 units were distributed in California and Texas. The FDA has classified this recall as Class II.
During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes. The source record does not describe a defect in the syringes themselves.
Affected product is lot 5268614 with an expiration date of 08/31/2030.
Facilities can identify affected product by the catalogue number, lot number and expiration date above, and may contact Becton Dickinson & Company for further information.
The recalled product
- Product
- 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
- Manufacturer
- Becton Dickinson & Company
- Category
- Medical Device — Syringe
- Hazard
- product-mixup
- packaging-error
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Catalog Number: 301029.
- UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.
Distribution
Distributed nationwide across the United States.
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