Medline recalls specific surgical drapes due to potential pouch packaging breach causing loss of sterility. Affected items include HEAD AND NECK OSIS, WILLIS SHOULDER PACK, and other surgical drape types. Consumers should check labels for listed model numbers and lot numbers.
Potential breach in pouch packaging which could lead to loss of sterility.
Medline is recalling certain sterile surgical drapes that may have packaging breaches leading to loss of sterility. This could cause infections during medical procedures if the drapes are used without proper sterility.
The pouch packaging may breach, causing the drape to lose sterility. If used during surgery without proper sterility, this could lead to infections in patients.
Healthcare professionals and surgical patients who use the recalled drapes for procedures. Those using the drapes in sterile environments are most at risk.
Check for model numbers DYNJ35520B, DYNJ38529F, DYNJ43406F, DYNJ43421D, DYNJ69185A, DYNJ69340B, DYNJ88923 or lot numbers listed in the recall notice. The drapes are labeled as HEAD AND NECK OSIS, WILLIS SHOULDER PACK, EXTREMITY PACK-LF, TOTAL HIP PACK-LF, SHOULDER W/POUCH-LF, or VEIN PACK.
Look for model numbers DYNJ35520B, DYNJ38529F, DYNJ43406F, DYNJ43421D, DYNJ69185A, DYNJ69340B, DYNJ88923 or lot numbers listed in the recall notice.
Medline is recalling specific sterile surgical drapes that may have packaging breaches leading to loss of sterility.
Check for model numbers DYNJ35520B, DYNJ38529F, DYNJ43406F, DYNJ43421D, DYNJ69185A, DYNJ69340B, DYNJ88923 or lot numbers listed in the recall notice.
The recall does not specify a remedy, so contact Medline directly for guidance.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1368-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-1368-2025 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.
