Medline Industries, LP: Device Recall

Recall #Z-1059-2026 · 11/26/2025

Class II: Risk

Recall Details

Recall Number
Z-1059-2026
Classification
Class II
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
11/26/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
12 units

Reason for Recall

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Product Description

Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935

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.