Z-2592-2025 Class I Ongoing
FDA device recall Z-2592-2025 was initiated by Medline Industries, LP on August 8, 2025 and is designated Class I. Reason for recall: Convenience kits labeled as sterile have not gone through the sterilization process. The recall status is ongoing. Affected quantity: 22 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 8, 2025
- Initiation Date
- August 8, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 22 units
Product Description
Sterile Medline Convenience Kits: 1) MAJOR PACK L-F, Model Number: DYNJ0382730O; 2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B
Reason for Recall
Convenience kits labeled as sterile have not gone through the sterilization process.
Distribution Pattern
US Distribution to States of: FL, MD, NJ, TN
Code Information
1) DYNJ0382730O, UDI-DI: 10198459117992(each), 40198459117993(case), Lot Number: 25GBC583; 2) DYNJ61038B, UDI-DI: 10195327596316(each), 40195327596317(case), Lot Number: 25GBF720;