Becton Dickinson recalls EU Kit BD Max Enteric Parasite Panel (Catalog #442960) due to unsealed foil bags that may cause contamination. Affected units include specific lot numbers and expiration dates.
The foil bags containing extraction tubes for BD MAX" Reagent products may not been sealed properly.
Becton Dickinson is recalling a specific enteric parasite test kit because the foil bags containing extraction tubes might not be sealed properly. This could lead to contamination of samples during testing, which might affect test accuracy.
The foil bags for extraction tubes may not be sealed properly, which could allow contaminants to enter the test samples. This might lead to inaccurate test results if the samples are not properly protected.
Users of the BD Max Enteric Parasite Panel EU test kit with the catalog number 442960 are affected. Laboratory staff and healthcare providers who use this kit for parasite testing are most at risk.
Check for the catalog number 442960 on the kit. The affected lot numbers include 9106889, and the expiration date is November 15, 2020.
Inspect the foil bags for proper sealing; if unsealed, do not use the kit.
This recall applies to the specific catalog number 442960 with lot number 9106889 and expiration date 11/15/2020. Check your kit's details to see if it matches.
Look for the catalog number 442960 on the kit. Affected units have lot number 9106889 and expire by November 15, 2020.
Inspect the foil bags for proper sealing. If unsealed, do not use the kit. Contact Becton Dickinson for further guidance.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2329-2019 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2329-2019 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.
