Recalled Medical Action Industries CentralLineDresChange Kit (Part 79420) has potential package integrity issues with BD ChloraPrep applicator. Consumers should check kit details and contact manufacturer for remedy.
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 their CentralLineDresChangeClrSeq kit due to a potential breach in the package integrity of the BD ChloraPrep 3mL applicator. This could lead to contamination or improper use of the medical device during patient care.
The kit contains a BD ChloraPrep 3mL applicator that may have compromised packaging, potentially leading to contamination or improper use during medical procedures. This could affect the safety of the medical device and patient care.
Healthcare professionals using the CentralLineDresChange kit for patient care are most at risk. Patients receiving this care may also be affected if the kit is used improperly.
Check for the kit part number 79420, which was sold with specific lot numbers (0000276767, 0000278361, 0000281458) between January 2022 and August 2022.
Look for the kit part number 79420 and lot numbers 0000276767, 0000278361, or 0000281458 on the packaging.
The recall is for Medical Action Industries CentralLineDresChangeClrSeq kit (part number 79420) due to potential package integrity issues with the BD ChloraPrep 3mL applicator.
Check the kit part number 79420 and lot numbers 0000276767, 0000278361, or 0000281458 on the packaging.
The recall record does not specify a remedy, so contact Medical Action Industries for further instructions.
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-1554-2021 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-1554-2021 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.
