Class II

Medical Device Recall: 10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.

Becton Dickinson & Company · January 27, 2026

Reason for Recall

During the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.

Distribution

US Nationwide distribution in the states of California and Texas.

States Affected

NATIONWIDE

Quantity Affected

204,000 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1496-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.