Medline recalls breast-hernia port convenience kits with Ferndale Laboratories MASTISOL Liquid Adhesive that 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 breast-hernia port convenience kits that contain a specific adhesive which can crack during use. This makes the kits unusable for applying medical devices.
The adhesive in these kits may crack during use, which can make the kits unusable for applying medical devices. This happens because the butyrate tubing is prone to cracking when the product is activated.
Patients using breast-hernia port kits with the specific model number CDS984853L are affected. Those who have the kits from the listed lots are most at risk.
Check for the model number CDS984853L on the kit. The kits were sold with lots 26AME511 and 26AMG737.
Look for the model number CDS984853L on the kit.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use, rendering the kits unusable for applying medical devices.
The affected model number is CDS984853L.
The affected lots are 26AME511 and 26AMG737.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2420-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2420-2026 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.
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