BD Vacutainer Eclipse Needles: Blood Leakage Risk from Missing Bevel

Take action

Contact the company & request your remedy

Recalling firmBecton Dickinson & Company1 Becton Dr · 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 Eclipse blood collection needles (22Gx1.25) because some have a missing bevel on the non-patient end, which can cause blood leakage. This could lead to inaccurate test results or unnecessary re-draws.

Why it’s dangerous

The needle's non-patient end lacks a bevel, causing blood to leak out during collection. This may result in inaccurate test results or requiring additional blood draws.

Who’s affected

Healthcare professionals and patients using these needles for blood draws. Those with the specific lot numbers listed are most at risk.

How to tell if you have this one

Check the product label for the model number 22Gx1.25 and lot numbers: 8207894, 9025826, 8354527, or 9010765. The product is sold by Becton Dickinson.

Brand
Becton Dickinson
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Needle Lot Number
Look for the lot number on the needle packaging or label to determine if it's affected.

✎ GovInfoNow

Questions people ask

Why is this recall happening?

Becton Dickinson received customer complaints that the non-patient needle end lacked a bevel, causing blood leakage.

What should I do if I have the affected needles?

The recall record does not specify a remedy, so contact Becton Dickinson directly for guidance.

Are there specific lot numbers I should check?

Yes, affected lots include 8207894, 9025826, 8354527, and 9010765.

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-0252-2020 — Becton Dickinson Becton Dickinson

Hello,

I own a Becton Dickinson that is covered by recall Z-0252-2020 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0252-2020 (March 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0252-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608

Lower-risk recall