Medline Industries, LP: Device Recall

Recall #Z-2593-2025 · 08/08/2025

Class I: Dangerous

Recall Details

Recall Number
Z-2593-2025
Classification
Class I
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
08/08/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
88 units

Reason for Recall

Convenience kits labeled as sterile have not gone through the sterilization process.

Product Description

Sterile Medline Convenience Kits: 1) EXTREMITY PACK, Model Number: DYNJ45701B

Distribution Pattern

US Distribution to States of: FL, MD, NJ, TN

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.