Medical Action Industries 306 recalls its Midline Insertion DA Kit (Part 77981B) due to potential package breach in BD ChloraPrep applicator. Affected kits have specific lot numbers and expiration dates. Consumers should contact the company for details.
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 its Midline Insertion DA Kit (Part Number 77981B) because a component's package might be compromised, risking contamination during medical procedures. This could lead to infections or other complications if the kit is used without proper safety.
The BD ChloraPrep 3mL applicator's package may have a breach, which could allow contamination during medical procedures. This might lead to infections or other complications if the kit is used without proper safety checks.
Healthcare professionals using the kit for medical procedures are most at risk. Patients receiving care with this kit could also be affected if the compromised component causes contamination.
Check for the kit part number 77981B on the packaging. Affected kits have lot numbers 0000281502 (expiring 04/08/2022), 0000282039 (expiring 04/08/2022), 0000274390 (expiring 07/09/2021), or 0000279101 (expiring 11/13/2021).
Look for the kit part number 77981B and lot numbers listed above on the packaging.
The recall is due to a potential package breach in the BD ChloraPrep applicator, which could lead to contamination during medical procedures. However, the risk is low and the company recommends checking the kit details.
Check for the kit part number 77981B and lot numbers 0000281502, 0000282039, 0000274390, or 0000279101 on the packaging.
The recall does not specify a remedy, so contact Medical Action Industries for details about the affected kits.
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-1556-2021 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-1556-2021 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.
