Medline recalls specific medical convenience kits due to higher-than-expected endotoxin levels in surgical patties and strips. Affected kits may pose a risk of infection during procedures.
Surgical Patties & Surgical Strips in specific lots of Custom Convenience Kits were found to contain higher-than-expected levels of endotoxin within the raw material used to produce sterile Codman Surgical Patties and Strips that may have resulted in out-of-specification levels of endotoxin in those finished goods
Medline is recalling certain medical procedure convenience kits that contain higher-than-expected endotoxin levels. This could increase the risk of infection during surgical procedures if the kits are used improperly.
The kits contain surgical patties and strips with elevated endotoxin levels from the raw materials. Endotoxins are bacterial components that can cause infections if they enter the body during medical procedures.
Healthcare professionals and medical facilities using the recalled Medline convenience kits are most at risk. Patients using these kits during procedures may face a higher infection risk.
Check for kits labeled with MVFF/FIBU #54-RF (SKU DYNJ21927R) or DIEP FLAP (SKU DYNJ910120A). The lot numbers listed in the recall include specific combinations like 23IBF547, 23GBT501, and others.
Look for the specific SKU and lot numbers listed in the recall to determine if your kit is affected.
The recall is due to higher-than-expected endotoxin levels in the surgical patties and strips, which could increase infection risk during medical procedures.
The risk is low; the endotoxin levels are higher than expected but not immediately dangerous under normal use conditions.
Check the product label for the specific SKU (DYNJ21927R or DYNJ910120A) and lot numbers listed in the recall.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-0721-2025 — Medline Medline Hello, I own a Medline that is covered by recall Z-0721-2025 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.
