Becton Dickinson BD Max Enteric Viral Panel Kit: Foil Bags May Not Seal Properly

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Recalling firmBecton Dickinson & Co.7 Loveton Cir, N/A · Sparks, MD 21152-9212

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Becton Dickinson is recalling a specific enteric viral panel kit because the foil bags containing extraction tubes might not seal correctly. This could lead to contamination or improper use of the reagents if the bags are compromised.

Why it’s dangerous

The foil bags for extraction tubes may not seal properly, which could allow contaminants to enter the reagents or cause improper handling. This might lead to inaccurate test results or potential cross-contamination in laboratory settings.

Who’s affected

Users of the BD Max Enteric Viral Panel EU Kit with the specified catalog number and lot numbers are affected. Laboratory personnel handling the kit are most at risk if the foil bags are not sealed properly.

How to tell if you have this one

Check for the catalog number 443985 on the kit label. Affected lots include 9085674 (expiring November 1, 2020) and 9107980 (expiring November 7, 2020).

Brand
Becton Dickinson
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Kit Label
Look for the catalog number 443985 and lot numbers 9085674 or 9107980 on the kit label.

✎ GovInfoNow

Questions people ask

What is the catalog number for the recalled kit?

The catalog number is 443985.

Which lots are affected?

Affected lots are 9085674 (expiring November 1, 2020) and 9107980 (expiring November 7, 2020).

How can I tell if my kit is recalled?

Check the kit label for catalog number 443985 and lot numbers 9085674 or 9107980.

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-2339-2019 — Becton Dickinson Becton Dickinson

Hello,

I own a Becton Dickinson that is covered by recall Z-2339-2019 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-2339-2019 (July 17, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2339-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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 & Co. recalls Kit BD Max Enteric Viral Panel EU Catalog # 443985

Lower-risk recall