Medline recalls labor and delivery C-section convenience kits with Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use, causing product failure.
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 labor and delivery C-section convenience kits that contain a specific adhesive which can crack during use, making the kit unusable. This could lead to improper medical procedures if the adhesive fails during critical moments.
The adhesive in these kits can crack during use, which may render the product unusable for medical applications. This could potentially lead to improper application during critical procedures like C-sections if the adhesive fails unexpectedly.
Healthcare workers using Medline's labor and delivery C-section convenience kits with the specific model number DYNJ907895F are most at risk. The recall affects kits sold with the UDI-DI 10198459366390 lot number.
Check for the model number DYNJ907:895F on the kit or the UDI-DI 10198459366390 lot number on the packaging. These kits were sold with the specific adhesive from Ferndale Laboratories.
Identify the model number DYNJ907895F on the kit or the UDI-DI 10198459366390 lot number on the packaging.
The kits contain Ferndale Laboratories MASTISOL Liquid Adhesive that may crack during use, rendering the product unusable for medical applications.
The official recall notice does not specify a remedy or action steps beyond checking the model number and lot number.
The recall states the adhesive may crack during use, but does not mention specific injury risks or mechanisms.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2429-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2429-2026 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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