Recall Z-2434-2026— Medline Industries, LP

Name: FDA recall Z-2434-2026
Creator: U.S. Food and Drug Administration
Published: 2026-04-27

Class II · Ongoing

Class II FDA medical device recall by Medline Industries, LP, initiated 2026-04-27. FDA's recall record names no specific 510(k) clearance for this event. Product: Medline convenience kits: DAVINCI MAIN DYNJ908031D. Reason: Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application..

Recalling firm: Medline Industries, LP
Classification: Class II
Status: Ongoing
Initiated: 2026-04-27
Firm location: Northfield, IL, United States

Product description

Medline convenience kits: DAVINCI MAIN DYNJ908031D

Reason for recall

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Data sourced from openFDA. This site is unofficial and independent of the FDA.