Becton Dickinson recalls BD Max ExK DNA 1 EU LUO kits with unsealed foil bags that may cause contamination. Affected kits have specific catalog and lot numbers. Consumers should contact the company for details.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Becton Dickinson is recalling BD Max ExK DNA 1 EU LUO kits because the foil bags containing extraction tubes might not be sealed properly. This could lead to contamination of samples during laboratory testing. Affected kits have specific catalog and lot numbers.
The foil bags for extraction tubes may not be sealed properly, which could allow contaminants to enter the samples during laboratory testing. This might lead to inaccurate test results if the samples are not properly protected.
Laboratory users who purchased the BD Max ExK DNA 1 EU LUO kits with catalog number 442818 and specific lot numbers. Those handling samples in clinical or research settings are most at risk.
Check for the catalog number 442818 and lot numbers 9085668 or 9106887 on the kit packaging. The kits were sold between 2010 and 2020 with expiration dates up to October 2020.
Look for the catalog number 442818 and lot numbers 9085668 or 9106887 on the kit packaging.
The foil bags containing extraction tubes may not be sealed properly, which could lead to contamination of samples during laboratory testing.
Check for the catalog number 442818 and lot numbers 9085668 or 9106887 on the kit packaging.
The recall does not specify a remedy, so contact Becton Dickinson for further instructions.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2324-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2324-2019 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.
