Medline recalls specific convenience kits due to butyrate tubing that may crack during use, rendering products unusable. Affected kits include ABD PACK DYNJ81673B and others listed in the recall.
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 kits unusable for application. This affects medical professionals and patients using these kits for procedures.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing in this adhesive may crack during use, which can render the product unusable for application. This does not pose an immediate risk of injury but affects the product's functionality.
Medical professionals and patients who use these kits for procedures like laparoscopy or bariatric surgery are most at risk. The recall applies to specific kits sold with unique model numbers and UDI codes.
Check for model numbers like DYNJ81673B (ABD PACK), DYNJ902515K (BARIATRIC), or CDS983883J (BARIATRIC CDS) on the kit. Also look for UDI codes such as 10195327494728 or 10195327662608.
Identify the model number on the kit, such as DYNJ81673B, DYNJ902515K, or CDS983883J.
Reach out to Medline Industries for assistance with the recall process using the model numbers and UDI codes listed.
The kits contain a recalled batch of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during use, rendering the product unusable for application.
Affected kits include ABD PACK DYNJ81673B, BARIATRIC DYNJ902515K, BARIATRIC + DYNJ904119O, and BARIATRIC CDS CDS983883J, among others listed in the recall.
Check the model number on the kit, such as DYNJ81673B, DYNJ902515K, or CDS983883J. Also look for UDI codes like 10195327494728 or 10195327662608.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2422-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2422-2026 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.
