Medline recalls convenience kits with Ferndale Laboratories MASTISOL Liquid Adhesive due to risk of butyrate tubing cracking during use, potentially rendering the product 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 specific convenience kits that contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. The adhesive's butyrate tubing may crack during use, making the product unusable for application.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing in this adhesive may crack during actuation, which can render the product unusable for application. This issue does not pose a direct risk of injury but affects the product's functionality.
Users of Medline convenience kits with the specific model numbers listed in the recall notice are affected. Healthcare professionals using these kits for medical adhesive applications are most at risk.
Check for the model numbers: CDS985505G, DYNJ68260D, DYNJ905094B, or CDS820091P on the kits. The recall includes specific lots from the Ferndale Laboratories MASTISOL product.
Identify the model number on the kit (CDS985505G, DYNJ68260D, DYNJ905094B, or CDS820091P) to confirm if it is recalled.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive where butyrate tubing may crack during use, rendering the product unusable.
The recall does not specify a remedy, so check the model numbers to see if it is affected and contact Medline for further instructions.
The recall states the tubing may crack, but it does not pose a risk of injury; the product becomes unusable instead.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2446-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2446-2026 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.
