Becton Dickinson recalls BD Max Vaginal Panel kits with unsealed foil bags that may cause contamination. Affected lots: 9092737, 9092738, 9127920. Expired 3/21/2020. Contact for remedy.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Becton Dickinson is recalling BD Max Vaginal Panel kits with catalog number 443712 because the foil bags containing extraction tubes might not be sealed properly. This could lead to contamination of samples during testing. Affected kits have specific lot numbers and expire by March 21, 2020.
The foil bags for extraction tubes may not be sealed properly, which could allow contaminants to enter the sample during testing. This might lead to inaccurate test results or contamination of the sample.
Users of BD Max Vaginal Panel kits with catalog number 443712 and lot numbers 9092737, 9092738, or 9127920 are affected. Healthcare professionals and individuals using these kits for vaginal sample testing are most at risk.
Check for the catalog number 443712 on the kit. Look for lot numbers 9092737, 9092738, or 9127920. The kits expire by March 21, 2020.
Look for lot numbers 9092737, 9092738, or 9127920 on the kit packaging.
The foil bags containing extraction tubes may not be sealed properly, which could lead to contamination of samples during testing.
The recall record does not specify a remedy, so contact Becton Dickinson directly for instructions.
Check for the catalog number 443712 and lot numbers 9092737, 9092738, or 9127920 on the kit packaging.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2336-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2336-2019 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.
