Medline recalls specific convenience kits due to potential butyrate tubing cracking, which could render the product unusable for ear surgery applications.
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 used in ear surgery procedures because the butyrate tubing inside may crack during use, making the product unusable. This could affect the safe application of the adhesive in medical procedures.
The kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing in these kits may crack during actuation, which can render the product unusable for proper application in ear surgery procedures.
Healthcare professionals using Medline convenience kits for ear surgery procedures are most at risk. Patients receiving these kits during surgery may be affected if the product becomes unusable.
Check for model numbers listed in the recall: DYNJ86476B, DYNJ81460C, DYNJ900004J, DYNJ901779J, DYNJ902900F, and others as detailed in the recall notice.
Identify the model number on the kit to see if it is listed in the recall.
The recall is happening because butyrate tubing in the kits may crack during use, rendering the product unusable for ear surgery applications.
The recall does not specify a remedy, so check the model numbers listed to see if your kit is affected and contact Medline for further instructions.
The recall states the product may become unusable, but does not mention a risk of serious injury or harm to users.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2421-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2421-2026 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.
