Z-0137-2026 Class II Ongoing
FDA device recall Z-0137-2026 was initiated by Medline Industries, LP on September 10, 2025 and is designated Class II. Reason for recall: Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking. The recall status is ongoing. Affected quantity: 950 units.
Recall Details
- Product Type
- Devices
- Report Date
- October 22, 2025
- Initiation Date
- September 10, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 950 units
Product Description
Medline Adult Anesthesia Set, REF DYNJ39985G
Reason for Recall
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
Distribution Pattern
US Nationwide distribution in the states of MO.
Code Information
UDI/DI 10198459062353 (EA) 40198459062354 (Case), Lot Numbers: 25GMB464