FDA Device recall Z-0137-2026
Medline Adult Anesthesia Set, REF DYNJ39985G
- FDA Device
- Class II
- ongoing
- Published 2025-10-22
On 2025-10-22 the FDA classified a Class II recall of Medline Adult Anesthesia Set, REF DYNJ39985G by Medline Industries, citing specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0137-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-09-10 |
| Published | 2025-10-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries |
| Distribution | US |
Product
Medline Adult Anesthesia Set, REF DYNJ39985G
Reason
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
Identifiers
| code_info | UDI/DI 10198459062353 (EA) 40198459062354 (Case), Lot Numbers: 25GMB464 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0137-2026%22
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