Medical Action Industries recalls sterile blue OR towels that may have compromised sterility. These hospital-grade towels are for blood and bodily fluid absorption. Affected items have specific lot numbers and expiration dates.
Product sterility potentially compromised.
Medical Action Industries is recalling sterile blue OR towels that may have compromised sterility. These towels are used for hand drying and blood/bodily fluid cleanup in medical settings. The recall is due to potential contamination risks during use.
The product's sterility could be compromised, meaning the towels might not be sterile when used. This could lead to infections if the towels come into contact with open wounds or sterile medical procedures. The risk is specific to medical environments where sterility is critical.
Healthcare workers and medical facilities using these sterile towels for blood and bodily fluid absorption. Patients receiving care in settings where these towels are used may be at risk if sterility is compromised.
Look for the product name 'Blue OR Towel Non X-Ray Detectable' with lot numbers 231479 (expiring 08/31/2021) or 232564 (expiring 11/06/2021). These towels are sold in packs of six and are intended for medical use only.
Verify the lot number and expiration date on the packaging to confirm if your towels are affected.
The recall states sterility may be compromised, so they should not be used until the remedy is applied. Medical facilities should follow their protocols for safe use.
The recall does not specify a remedy, so contact the manufacturer directly for guidance on handling affected items.
Check for lot numbers 231479 (expiring 08/31/2021) or 232564 (expiring 11/06/2021) on the packaging.
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-2043-2018 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-2043-2018 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.
