Medline recalls Quick-Strip sterile bandages due to potential open packaging that could compromise sterility. Affected lots include all units sold with specific item numbers.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.
Medline is recalling Quick-Strip sterile bandages because their packaging might have open seals, risking contamination. This means the bandages could be less sterile than they should be, which is especially important for medical use.
The bandages' packaging may have open seals, which could allow contamination. This might make the bandages less sterile than intended, especially for medical use where sterility is critical.
People who own or use Medline Quick-Strip bandages with the specific item numbers listed in the recall are affected. Those using the bandages for medical purposes are at higher risk due to potential sterility issues.
Check for the Medline Quick-Strip bandages with the item numbers listed in the recall: UDI/DI 10888277699397 (each), 208888277699394 (box), 30888277699391 (case). All lots are affected.
Look for open seals on the packaging of the bandages to determine if they might be compromised.
Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may have open seals in the packaging that could compromise sterility.
Check for the Medline Quick-Strip bandages with item numbers: UDI/DI 10888277699397 (each), 20888277699394 (box), 30888277699391 (case). All lots are affected.
The recall record does not specify a remedy, so there is no action required beyond checking for open seals in the packaging.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0900-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0900-2026 from Medline. 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.
