Becton Dickinson BD Max MRSA Kit Recall: Foil Bags Not Sealed 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 their BD Max MRSA Kit (Catalog #442953) because the foil bags holding extraction tubes might not be sealed correctly. This could cause contamination if the tubes are used without proper sealing.

Why it’s dangerous

The foil bags containing extraction tubes for BD MAX reagent products may not be sealed properly. This could lead to contamination if the tubes are used without the correct seal, potentially affecting test results or causing cross-contamination.

Who’s affected

Users of the BD Max MRSA Kit (Catalog #442953) who purchased it between 2019 and 2019 are affected. Laboratory personnel and healthcare professionals using this kit are at higher risk due to potential contamination.

How to tell if you have this one

Check for the BD Max MRSA Kit with Catalog #442953. The kit was sold with Lot #9071522 and expired on December 19, 2019. The UDI (GTIN) is (01)00382904429539.

Brand
Becton Dickinson
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the Catalog #442953 and Lot #9071522 on the kit packaging.

✎ GovInfoNow

Questions people ask

Is this kit safe to use?

The recall states the foil bags may not be sealed properly, which could lead to contamination risks. However, the remedy is not specified, so users should check the product details before use.

What should I do if I have this kit?

The recall record does not specify a remedy, so users should check the product details to determine if they have the affected kit.

When was this kit sold?

The kit was sold with Lot #9071522 and expired on December 19, 2019.

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-2328-2019 — Becton Dickinson Becton Dickinson

Hello,

I own a Becton Dickinson that is covered by recall Z-2328-2019 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-2328-2019 (July 17, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2328-2019 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 MRSA; Catalog # 442953

Lower-risk recall