Medline Industries, LP: Device Recall

Recall #Z-1196-2026 · 12/12/2025

Class II: Risk

Recall Details

Recall Number
Z-1196-2026
Classification
Class II
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
12/12/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
236 units

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.

Product Description

Medline medical procedure convenience kits labeled as: 1) DEPAUL BASIC NEURO-LF, Kit SKU DYNJ20028L; 2) NEURO MINOR PACK, Kit SKU DYNJ46546M; 3) NEURO SHUNT PACK, Kit SKU DYNJ54396K; 4) NEURO PACK, Kit SKU DYNJ59397Q; 5) NEURO BASIC, Kit SKU DYNJ904052L; 6) PK NEURO SHUNT BUMC, Kit SKU DYNJT6428.

Distribution Pattern

US Nationwide distribution.

Other Recalls by Medline Industries, LP

View all recalls by Medline Industries, LP →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.