Medline recalls several breast imaging and augmentation kits due to potential butyrate tubing cracking, which could render products unusable for application.
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 multiple breast imaging and augmentation kits because the butyrate tubing inside may crack during use, making the products unusable. This could affect medical procedures requiring precise application of the adhesive.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing in these kits can crack during actuation, which means the adhesive might not apply correctly. This could lead to the product being unusable for medical procedures.
Healthcare professionals using Medline's breast imaging or augmentation kits are likely affected. Those with the specific model numbers listed in the recall are at risk of using a product that may not work properly.
Check for model numbers like DYNJT5893, SYNJ10306A, DYNJ68023, and others listed in the recall. The kits were sold with specific lot numbers such as 25KBA123, 25LBO305, and 26CBD081.
Identify the model number on the kit to see if it matches the recalled list.
Reach out to Medline directly for guidance on whether your kit is affected and what to do next.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive, and butyrate tubing may crack during use, rendering the product unusable for application.
Affected model numbers include DYNJT5893, SYNJ10306A, DYNJ68023, DYNJ909926C, DYNJ84081B, DYNJ905362C, DYNJ0660040R, DYNJ89023A, DYNJ902510M, DYNJ84766, DYNJ0578842M, DYNJ63803C, DYNJ62433D, DYNJ81772C, DYNJT7588, and DYNJ89048A.
Check the model number on the kit against the list provided in the recall. Also, verify the lot numbers such as 25KBA123, 25LBO305, or 26CBD081.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2423-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2423-2026 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.
