CLASS II ONGOING Device recall · Reported 18 Mar 2026 · FDA Enforcement Report

Non-Sterile BD Luer-Lok Tip Syringe Only recalled by Becton Dickinson &

Becton Dickinson is recalling Non-Sterile BD Luer-Lok Tip Syringe Only, distributed nationwide in the US. The recall was initiated on 27 Jan 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesCatalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.

Quantity recalled204,000 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-1496-2026
FDA event ID: 98314
Recalling firm: Becton Dickinson, Franklin Lakes, NJ
Classification: Class II
Status: Ongoing
Recall initiated: 27 Jan 2026
FDA classified: 6 Mar 2026
Reported: 18 Mar 2026
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Packaging Defects
Device type: Syringes & Needles

Timeline

27 Jan 2026	Recall initiated by company
6 Mar 2026	Classified by FDA	+38 days
18 Mar 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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

Where it was distributed

US Nationwide distribution in the states of California and Texas.

Nationwide California Texas

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Catalog Number: 301029., UDI-DI: N/A. Lot Number: 5268614. Expiration Date: 08/31/2030.

Where was it sold?

US Nationwide distribution in the states of California and Texas.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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