Medline Industries, LP: Device Recall

Recall #Z-0137-2026 · 09/10/2025

Class II: Risk

Recall Details

Recall Number
Z-0137-2026
Classification
Class II
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
09/10/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
950 units

Reason for Recall

Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.

Product Description

Medline Adult Anesthesia Set, REF DYNJ39985G

Distribution Pattern

US Nationwide distribution in the states of MO.

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.