Recalled Medical Action Industries Blood Culture Kit (Part 80076) has potential package breach risk. Affected kits may have compromised BD ChloraPrep 3mL applicator. Stop using immediately if you own this kit.
Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD ChloraPrep 3mL applicator.
Medical Action Industries is recalling blood culture kits with part number 80076 due to a possible breach in the package integrity of the BD ChloraPrep 3mL applicator. This could lead to contamination or improper use of the kit during medical procedures.
The package integrity of the BD ChloraPrep 3mL applicator may be compromised, potentially leading to contamination or improper use of the blood culture kit during medical procedures. This could affect the accuracy of blood culture results and patient safety.
Healthcare professionals and medical facilities that use the recalled blood culture kits. Those handling the BD ChloraPrep 3mL applicator are most at risk.
Check for the kit part number 80076. The kit may have lot numbers 0000280292, 0000280766, 0000281206, 0000279153, or 0000280969 with specific expiration dates.
Verify the kit part number is 80076 and check the lot numbers listed in the recall notice.
The BD ChloraPrep 3mL applicator in the blood culture kit.
Check for the kit part number 80076 and lot numbers 0000280292, 0000280766, 0000281206, 0000279153, or 0000280969.
The recall does not specify an immediate stop-use action, but you should check the kit details to confirm if it is affected.
We’ve drafted a message you can send Medical Action Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1559-2021 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-1559-2021 from Medical Action Industries. 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.
