Recall Z-1496-2026— Becton Dickinson & Company

Name: FDA recall Z-1496-2026
Creator: U.S. Food and Drug Administration
Published: 2026-01-27

Class II · Ongoing

Class II FDA medical device recall by Becton Dickinson & Company, initiated 2026-01-27. It names one FDA 510(k) clearance: K980987. 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..

Recalling firm: Becton Dickinson & Company
Classification: Class II
Status: Ongoing
Initiated: 2026-01-27
Firm location: Franklin Lakes, NJ, United States

510(k) clearances named in this recall

1 on FDA's record

K980987 — BECTON DICKINSON SYRINGEBd Becton Dickinson Vacutainer Systems Preanalytic·cleared 1998-06-11

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.