Medline recalls specific convenience kits due to potential butyrate tubing cracking, which could render products unusable for application. Affected kits include DAVINCI DYNJ905836D 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 certain convenience kits that contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack during use, making the kits unusable for medical applications.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive with butyrate tubing that may crack during actuation. This cracking could render the product unusable for application, potentially affecting surgical procedures.
Healthcare professionals using Medline convenience kits for surgical procedures are most at risk. The recall affects specific kits sold with certain model numbers and lot codes.
Check the model numbers listed in the recall: DAVINCI DYNJ905836D, DAVINCI-LF DYNJ905293I, GENERAL ROBOTICS PACK DYNJT8308, and others. Also look for the lot codes like 25LBB534 or 25KBM585.
Identify the model numbers listed in the recall, such as DAVINCI DYNJ905836D or DYNJ905293I.
Reach out to Medline directly to confirm if your kit is affected and get instructions.
The kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive where butyrate tubing may crack during actuation, rendering the product unusable.
Check the model numbers and lot codes listed in the recall, such as DAVINCI DYNJ905836D with lot 25LBB534 or DYNJ905293I with lot 25KBM585.
Contact Medline directly to confirm if your kit is affected and get instructions for 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-2431-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2431-2026 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.
