Medline recalls sterile 5.5" scissors with weak packaging seals that could breach sterility, increasing infection risk. Affected items have specific item numbers and were sold in 2023. Consumers should check labels for item number DYND04000.
The items may have weak packaging seals that may result in a breach of sterility if the seal fails and may lead to an increased risk of infection if product is utilized.
Medline is recalling sterile 5.5-inch scissors that may have weak packaging seals. If the seal fails, the scissors could become contaminated, increasing infection risk during medical procedures.
The scissors' packaging seals might fail, allowing contamination. If the seal breaks, the scissors could no longer be sterile, increasing the risk of infection during medical procedures.
Healthcare professionals and medical facilities using these scissors for procedures are most at risk. The recall affects specific items sold with item number DYND04000.
Check for item number DYND04000 on the scissors packaging. The scissors were sold in 2023 with lot number 2023102590.
Look for item number DYND04000 on the scissors packaging or label.
The scissors may have weak packaging seals that could breach sterility, increasing infection risk if used after the seal fails.
Check for item number DYND04000 on the scissors packaging or label. The scissors were sold in 2023 with lot number 2023102590.
The recall record does not specify a remedy, so check with Medline Industries 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-0921-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-0921-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
