Medline recalls basic eye and tubal ligation kits with Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during use, rendering kits unusable.
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 basic eye and tubal ligation kits that contain Ferndale Laboratories MASTISOL Liquid Adhesive. The kits may have butyrate tubing that cracks during use, making them unusable for application.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation, which can render the product unusable for application. This could lead to failed medical procedures if the tubing is not functional.
People who own or use Medline convenience kits with the specific model numbers DYNJ905154I and CDS760053K are affected. Those who use these kits for medical procedures may be at risk if the tubing cracks.
Check for model numbers DYNJ905154I or CDS760053K on the kit. The kits were sold with specific lots: DYNJ905154I lots 26ABB308 and 26BBA671, and CDS760053K lot 25KBP010.
Look for model numbers DYNJ905154I or CDS760053K on the kit.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during use, rendering the product unusable for application.
The recall record does not specify a remedy, so no action is required beyond checking if you have the affected model numbers.
Check for model numbers DYNJ905154I or CDS760053K. Affected kits were sold with specific lots: DYNJ905154I lots 26ABB308 and 26BBA671, and CDS760053K lot 25KBP010.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2435-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2435-2026 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.
