Medical Action Industries recalls 306 Injection Review Kit (Part 74736) due to potential package breach in BD ChloraPrep applicator. Affected units sold through specific channels until 02/28/2022.
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 306 Injection Review Kit (Part Number 74736) because the packaging for the BD ChloraPrep 3mL applicator might be compromised. This could lead to contamination risks if the kit is used improperly.
The BD ChloraPrep 3mL applicator's packaging may have a breach, potentially allowing contamination of the solution. This could happen if the kit is used without proper protection from the breach.
Healthcare professionals and medical facilities that purchased the 306 Injection Review Kit with Part Number 74736. Those using the kit for injections are most at risk if the packaging is compromised.
Check for the Part Number 74736 on the kit. The kit was sold with Lot Number 0000266521 and expired February 28, 2022.
Look for the Part Number 74736 on the kit label to confirm if it's affected.
The recall is due to potential packaging issues with the BD ChloraPrep applicator, but the kit itself is not inherently dangerous. The risk is low if the packaging is intact.
Check for the Part Number 74736 on the kit. The affected units were sold with Lot Number 0000266521 and expired February 28, 2022.
The recall does not specify a remedy, so no action is required unless you notice packaging issues. Contact the manufacturer for further guidance.
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-1555-2021 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-1555-2021 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.
