Becton Dickinson recalls BD Max Enteric Viral Panel RUO kits with catalog #443715 due to foil bags not sealing properly. This could lead to contamination of reagents. Consumers should check product details and contact the company for instructions.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Becton Dickinson is recalling a specific enteric viral panel kit because the foil bags containing extraction tubes might not seal properly. This could lead to contamination of the reagents, which might affect test accuracy or safety.
The foil bags may not seal properly, which could allow contamination of the extraction tubes. This might lead to inaccurate test results or potential cross-contamination of reagents.
Users of the BD Max Enteric Viral Panel RUO kit with catalog number 443715 are affected. Laboratory personnel and healthcare providers who use this kit for testing are most at risk.
Check for the catalog number 443715 on the kit. The lot number 9114647 and expiration date 11/7/2020 are also listed on the product.
Look for the catalog number 443715, lot number 9114647, and expiration date 11/7/2020 on the kit.
The recall states that the foil bags may not seal properly, which could lead to contamination. However, the remedy is not specified, so it's recommended to check the product details and contact Becton Dickinson for further instructions.
The recall does not specify a remedy, so you should check the product details and contact Becton Dickinson for instructions on next steps.
Check for the catalog number 443715, lot number 9114647, and expiration date 11/7/2020 on the kit.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2337-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2337-2019 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.
