Medline Adult Anesthesia Set — Class II medical device recall Z-0137-2026
Ongoing recall by Medline Industries, LP, reported 2025-10-22, distributed nationwide. Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer re
| Recall number | Z-0137-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Medline Industries, LP, Northfield, IL, United States |
| Recall initiated | 2025-09-10 |
| Classified | 2025-10-10 |
| Reported by FDA | 2025-10-22 |
| Distributed | Nationwide (US) |
| Quantity | 950 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 10198459062353, 40198459062354 |
| Lot numbers | 25GMB464 |
| Model numbers | DYNJ39985G |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0137-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.