Becton Dickinson 10mL Non-Sterile Luer-Lok Syringes Recalled Due to Wrong Syringe Type

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Contact the company & request your remedy

Recalling firmBecton Dickinson & Company1 Becton Dr, N/A · Franklin Lakes, NJ 07417-1815

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Becton Dickinson is recalling 850 units of 10mL non-sterile Luer-Lok Tip Syringes (Catalog 301029) because some Luer Slip syringes were incorrectly included in the batch. This could lead to using the wrong type of syringe, which may cause errors in medical procedures.

Why it’s dangerous

During bulk packaging, some Luer Slip syringes were mistakenly included in a batch intended for Luer-Lok syringes. This mix-up could lead to using the wrong syringe type, potentially causing errors in medical procedures.

Who’s affected

Healthcare professionals and individuals using these syringes for medical purposes are likely affected. Those who have the specific catalog number 301029 and lot number 5268614 are most at risk.

How to tell if you have this one

Check for the catalog number 301029 and lot number 5268614 on the syringe packaging. The product is a 10mL non-sterile Luer-Lok Tip Syringe sold in bulk cases of 850 units.

Brand
Becton Dickinson
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Syringe Details
Look for the catalog number 301029 and lot number 5268614 on the syringe packaging.

✎ GovInfoNow

Questions people ask

What is the catalog number for the recalled syringes?

The catalog number is 301029.

What lot number is affected?

The lot number is 5268614.

How many units are being recalled?

850 units of 10mL non-sterile Luer-Lok Tip Syringes.

Take action

Contact Becton Dickinson

We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1496-2026 — Becton Dickinson Becton Dickinson

Hello,

I own a Becton Dickinson that is covered by recall Z-1496-2026 from Becton Dickinson.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-1496-2026 (January 27, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1496-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

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

Lower-risk recall