Medline recalls FEMORAL BLOCK TRAY kits with DYNJRA1739B model due to butyrate tubing that may crack during use, rendering adhesive 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 convenience kits with the FEMORAL BLOCK TRAY model DYNJ:1739B because the butyrate tubing inside can crack during use, making the adhesive unusable. This could lead to improper medical application if the kit is used without the adhesive working correctly.
The butyrate tubing in the kits can crack during use, which makes the MASTISOL Liquid Adhesive unusable for medical applications. This could lead to improper application of the adhesive during procedures if the kit is used without the adhesive working correctly.
Healthcare professionals using Medline's FEMORAL BLOCK TRAY kits with model DYNJRA1739B are most at risk. Patients receiving procedures using these kits may also be affected if the adhesive fails.
Check for the model number DYNJRA1739B on the kit. The kits were sold with lot number 25LBB731 and were distributed by Medline Industries, LP.
Look for the model number DYNJRA1739B on the kit label.
The butyrate tubing in the kits can crack during use, rendering the MASTISOL Liquid Adhesive unusable for medical applications.
The recall record does not specify a remedy, so no action is required beyond checking if you have the model DYNJRA1739B.
The recall indicates the tubing may crack, making the adhesive unusable, but the record does not specify a risk of injury or serious harm.
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2442-2026 — Medline Medline Hello, I own a Medline that is covered by recall Z-2442-2026 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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