FDA recall Z-1496-2026

Becton Dickinson & Company · Class II · device

Product

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

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.

Key facts

Status
Ongoing
Initiation date
2026-01-27
Report date
2026-03-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
Franklin Lakes, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1496-2026