Medline recalls minor cath lab packs and vascular angio packs with butyrate tubing that may crack during use, rendering products unusable. Affected lots include DYNJ84775A lot 25LMH070 and others.
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Medline is recalling minor cath lab packs and vascular angio packs that contain tubing which may crack during use. This could make the products unusable for medical applications.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation, which can render the product unusable for application.
Healthcare professionals using these specific cath lab packs or vascular angio packs for medical procedures are most at risk. Patients receiving these products may be affected if the tubing cracks.
Check for the product model numbers DYNJ84775A (lot 25LMH070), DYNJ47269D (lot 25LMJ234), or DYNJ63276G (lot 26BBC598). These are the specific affected lots.
Identify the lot number on the product label to see if it matches the affected lots listed: DYNJ84775A lot 25LMH070, DYNJ47269D lot 25LMJ234, or DYNJ63276G lot 26BBC598.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation, which can render the product unusable for medical applications.
Check for the product model numbers DYNJ84775A (lot 25LMH070), DYNJ47269D (lot 25LMJ234), or DYNJ63276G (lot 26BBC598).
The recall does not specify a remedy, so contact Medline directly for guidance on next steps.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2417-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2417-2026 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.