Becton Dickinson recalls BD Max Cdiff EU kits with unsealed foil bags that may cause contamination. Affected units include Catalog # 442: 9127912. Consumers should check product labels for the serial number.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Becton Dickinson is recalling BD Max Cdiff EU kits because the foil bags containing extraction tubes might not be sealed properly. This could lead to contamination of samples during testing, which may affect test accuracy. Affected kits have a specific catalog number and lot number.
The foil bags for extraction tubes may not be sealed properly, which could allow contaminants to enter the samples. This might lead to inaccurate test results if the samples are exposed to external substances.
Users of BD Max Cdiff EU kits for stool testing are affected. Those who have the kit with catalog number 442555 and lot number 9127912 are most at risk.
Check the kit's catalog number (442555) and lot number (9127912) on the label. The unique identifier (UDI) starts with (01)00382904425555.
Look for the catalog number 442555 and lot number 9127912 on the kit's label.
The foil bags containing extraction tubes may not be sealed properly, which could lead to contamination of samples during testing.
Check the kit's label for the catalog number 442555 and lot number 9127912. If it matches, contact Becton Dickinson for further instructions.
The recall addresses potential contamination of samples, not physical injury. This is a low-risk issue.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2322-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2322-2019 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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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.
