Medline recalls 28 medical procedure kits with MASTISOL liquid adhesive that cracks during vial actuation, potentially causing leaks. Check your kit's SKU and lot number for affected models.
Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
Medline is recalling 28 different medical procedure kits because the MASTISOL liquid adhesive inside can crack when the vials are used, which might lead to leaks. This could pose a risk of contamination or improper medical procedures if the adhesive leaks.
The MASTISOL liquid adhesive in the kits can crack when the vials are activated, potentially causing leaks. This could lead to contamination or improper medical procedures if the adhesive leaks during use.
Healthcare professionals and medical facilities that use these kits are most at risk. Patients using these kits during procedures may be affected if the adhesive leaks.
Check for kits labeled with specific SKUs listed in the recall, such as DYNJ0275635M, DYNJ0395037X, and others. Look for lot numbers like 25KMH120, 25LMB119, etc.
Identify your kit's SKU and lot number to confirm if it's affected by this recall.
The recall includes 28 specific medical procedure kits with SKUs like DYNJ0275635M, DYNJ0395037X, and others, each with unique lot numbers.
The recall does not specify a remedy, so you should check with Medline directly for guidance on handling affected kits.
The recall states that the adhesive can crack during use, but no specific injuries or serious risks are mentioned, so the risk is considered low.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1200-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1200-2026 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.
