Medline Industries, LP: Device Recall
Recall #Z-2592-2025 · 08/08/2025
Class I: Dangerous
Recall Details
- Recall Number
- Z-2592-2025
- 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
- 22 units
Reason for Recall
Convenience kits labeled as sterile have not gone through the sterilization process.
Product Description
Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B
Distribution Pattern
US Distribution to States of: FL, MD, NJ, TN
Other Recalls by Medline Industries, LP
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
- Class II: Risk 12/16/2025
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.