Medline recalls sterile povidone solution with non-sterile contents. Products sold with lot numbers 2:2022040790 or 2022062190 may be affected. Contact for remedy details.
The product description on the labeling includes the word "Sterile" or STRL", however the contents of the solution inside the foil sachet is non-sterile.
Medline is recalling sterile povidone solution because the actual contents inside the foil sachet are non-sterile. This means the product does not meet its claimed sterile status, which could lead to infection risks if used for medical purposes.
The product is labeled as 'sterile' but contains non-sterile solution inside the foil pouch. This could lead to infection if the product is used for medical procedures where sterility is critical. However, the risk is limited to medical use cases.
Healthcare professionals and medical facilities using this product for wound care or similar applications. Individuals using it for non-medical purposes are less likely to be affected.
Check the lot numbers on the packaging: 2022040790 or 2022062190. The product is labeled as 'Sterile' or 'STRL' but contains non-sterile solution.
Look for lot numbers 2022040790 or 2022062190 on the packaging.
The product is labeled as sterile but contains non-sterile solution. It is not safe for medical use where sterility is required.
The recall record does not specify a remedy, so contact Medline directly for guidance.
Check the lot numbers: 2022040790 or 2022062190. The product is labeled as 'Sterile' or 'STRL' but contains non-sterile solution.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0531-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0531-2024 from Medline 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.
