Medline recalls medical procedure kits with MASTISOL liquid adhesive that cracked during use, posing a risk of leaks or contamination. Affected kits have 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 several medical procedure kits because the MASTISOL liquid adhesive inside can crack during use, potentially causing leaks or contamination. This could lead to improper medical procedures or infections if the kits are used without the adhesive being intact.
The MASTISOL liquid adhesive in these kits can crack when the vials are actuated, which means it might leak or contaminate medical equipment. This could lead to improper medical procedures or infections if the adhesive is not properly sealed.
Healthcare professionals using Medline medical procedure kits with the listed SKUs and lot numbers are most at risk. Patients receiving procedures using these kits may also be affected if the adhesive cracks.
Check the kit's SKU number and lot number on the packaging. Affected kits include specific models like PACER / CATH LAB PACK-LF (SKU DYNJ0972604A) with lot numbers starting with 25KMD.
Identify the SKU and lot number on the kit packaging to confirm if it is affected.
The MASTISOL liquid adhesive in these kits can crack during use, potentially causing leaks or contamination.
Check the SKU and lot number on the packaging to see if it is affected. If it is, stop using it and contact Medline for further instructions.
Yes, affected models include PACER / CATH LAB PACK-LF (SKU DYNJ0972604A) and others with specific lot numbers starting with 25KMD.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-1188-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-1188-2026 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.
