Medline recalls 62 medical procedure convenience kits with MASTISOL liquid adhesive that cracked during use, potentially causing leaks. Affected kits include drawer 1 airway and others with specific SKUs and lot numbers.
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 62 medical procedure convenience kits that contain MASTISOL liquid adhesive. The adhesive's butyrate tubing can crack during use, which may lead to leaks. This is a safety issue for medical professionals handling these kits.
The MASTISOL liquid adhesive in these kits contains butyrate tubing that can crack when activated. This cracking may cause leaks of the adhesive, which could lead to contamination or other issues during medical procedures.
Medical professionals who use these kits in clinical settings are most at risk. The recall affects Medline's medical procedure convenience kits sold with specific SKUs and lot numbers.
Check for Medline medical procedure convenience kits with SKUs listed in the recall, such as ACC010270A or DYNJ00282Q. Look for lot numbers starting with 25LDA, 25KMC, or similar prefixes.
Identify your kit's SKU and lot number from the product labels. Compare with the list of affected SKUs and lot numbers provided in the recall.
The recall is due to complaints that the butyrate tubing in the MASTISOL liquid adhesive cracks during actuation, which may cause leaks.
Check the SKU and lot number on your kit. Affected kits have specific SKUs like ACC010270A or DYNJ00282Q with lot numbers starting with 25LDA, 25KMC, or similar prefixes.
The recall does not specify a remedy, so you should check with Medline directly for guidance on handling affected kits.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1193-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1193-2026 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.
