Class II

Medical Device Recall: Medline medical procedure convenience kits labeled as: HEAD SHAVE-LATEX SAFE KIT, Kit SKU P903933B

Medline Industries, LP · December 12, 2025

Reason for Recall

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.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

60 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1194-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.