Medline recalls Sterile Betadine solution with non-sterile contents. Affected lots from 2021-2023 may cause infection if used for medical purposes.
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 Betadine solution because the product label says 'sterile' but the actual solution inside the foil sachet is non-sterile. Using this product for medical purposes could lead to infection.
The product label claims the solution is sterile, but the actual contents are non-sterile. This means the solution could cause infection if used for medical purposes like wound cleaning.
People who purchased Sterile Betadine solution with lot numbers from 2021042190 to 2022031090 are affected. Medical users are most at risk.
Check the lot number on the foil pouch. Affected lots include 2021100490, 2022011290, 2022031090, 2022041390, 2022081590, 2022101090, and 2023042190.
Look for the lot number on the foil pouch, which should be one of the listed numbers: 2021100490, 2022011290, 2022031090, 2022041390, 2022081590, 2022101090, or 2023042190.
The product label says 'sterile' but the actual solution is non-sterile, so it may cause infection if used for medical purposes. Do not use for medical purposes.
Check the lot number on the foil pouch. If it matches the affected lots listed, stop using it and contact Medline for instructions.
Look for lot numbers on the foil pouch: 2021100490, 2022011290, 2022031090, 2022041390, 2022081590, 2022101090, or 2023042190.
We’ve drafted a message you can send Medline Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-0530-2024 — Medline Industries Medline Industries Hello, I own a Medline Industries that is covered by recall Z-0530-2024 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.
