Medline Industries, LP: Device Recall

Recall #Z-1188-2026 · 12/12/2025

Class II: Risk

Recall Details

Recall Number
Z-1188-2026
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
1,928 total

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) PACER / CATH LAB PACK-LF, Kit SKU DYNJ0972604A; 2) PACEMAKER/ICD PACK, Kit SKU DYNJ33822L; 3) VENOUS ACCESS PACK, Kit SKU DYNJ45640B; 4) PACEMAKER SET UP, Kit SKU DYNJ63377D; 5) PACK PACEMAKER CUSTOM,9909178, Kit SKU DYNJ65011D; 6) HEART BASIC OPEN PACK, Kit SKU DYNJ69143C; 7) SCC VEIN PACK, Kit SKU DYNJ69313; 8) CV PACK, Kit SKU DYNJ86007B.

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.