Home/Recalls/FDA-Z-1496-2026
FDA DevicesClass II

10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk ...

Published: March 18, 2026Recall ID: Z-1496-2026Category: devicesCountry: US

Reason for Recall / Hazard

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

Product Description & Identification

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

Additional Source Details

FieldValue
CityFranklin Lakes
StateNJ
Event id98314
Address 11 Becton Dr
Address 2N/A
Code infoCatalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.
Postal code07417-1815
Report date20260318
Product typeDevices
Product quantity204,000 units
Reason for recallDuring the bulk packaging process, some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260127
Initial firm notificationE-Mail
Center classification date20260306

Overview

  • Recalling FirmBecton Dickinson & Company
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of California and Texas.
Official Agency Alert