Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.
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Recall Number
Z-1186-2026
Classification
Class II
Status
Ongoing
Category
device
Initiated
2025-12-12
Reported
2026-02-04
Distribution
US Nationwide distribution.
Code Info
UDI/DI 10198459565861 (EA) 40198459565862 (CS), Lot number 25KMD285
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.