Medical Action Industries recalls certain CVC Clear Sequence Change Kits due to saline solution pH potentially exceeding USP standards (4.5-7.0). Affected kits include specific models and lot numbers listed in the recall notice.
The kits contain a bottle of saline solution which may exceed the USP specified pH requirements of 4.5-7.0.
Medical Action Industries is recalling several types of medical convenience trays and kits, including CVC Clear Sequence Change Kits, because the saline solution inside may have a pH outside the safe range (4.5-7.0) as per USP standards. This could potentially cause issues with medical treatments.
The saline solution in the kits may have a pH outside the USP-specified range of 4.5 to 7.0. This could potentially affect the effectiveness of the saline solution in medical procedures, though the recall does not specify serious injury risks.
Healthcare professionals and patients using the recalled kits for medical procedures like dressing changes or wound care. Those most at risk are individuals with central lines or tracheostomies who use these kits regularly.
Check for the product names listed in the recall, such as 'CVC Clear Sequence Change Kit', 'Dialysis Clear Sequence Change Kit', and others. Look for specific lot numbers like 0000250140 or 0000250814 on the packaging.
Identify the product name and lot number on the packaging to confirm if it's affected by this recall.
The recall does not specify a need to stop using the kits immediately. The hazard is described as a potential pH issue, which is not stated to cause serious injury.
The recall does not provide a specific remedy or action steps for affected products. You should check the product details to confirm if your kit is affected.
Check the product name and lot number on the packaging against the list of affected products and lot numbers provided in the recall notice.
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-0779-2020 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-0779-2020 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.
