Medline recalls C-Section kits with Ferndale Laboratories MASTISOL Liquid Adhesive that may crack butyrate tubing, rendering kits unusable for surgical 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 two specific C-Section surgical kits because they contain a batch of adhesive that can crack during use, making the kits unusable for medical procedures. This poses a risk to patients during surgery if the kits fail to function properly.
The kits contain a specific batch of Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use. This cracking can render the butyrate tubing unusable, potentially causing the surgical kit to fail during critical procedures.
Surgical teams and hospitals using the recalled Medline C-Section kits (model DYNJ904305J and DYNJ69533C) are most at risk. Patients undergoing surgery with these kits could face complications if the adhesive fails.
Check for the model numbers DYNJ904305J or DYNJ69533C on the kits. The kits were sold with specific lot numbers: DYNJ904305J lot 25KBT972 and DYNJ69533C lot 26BBC483.
Identify the model number on the kit (DYNJ904305J or DYNJ69533C) to confirm if it's affected.
Reach out to Medline directly for guidance on next steps if you have the recalled kits.
The kits contain a specific batch of Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use, rendering the butyrate tubing unusable for surgical applications.
Check for model numbers DYNJ904305J or DYNJ69533C with lot numbers 25KBT972 or 26BBC483 respectively.
Contact Medline directly for guidance on next steps, as the recall does not include a specific remedy.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2432-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2432-2026 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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