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
- 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.