Namic FLUID DELIVERY SET — Class II medical device recall Z-1807-2024
Ongoing recall by MEDLINE INDUSTRIES, LP - Northfield, reported 2024-05-22, distributed nationwide. Products have a lack of sterility assurance.
| Recall number | Z-1807-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MEDLINE INDUSTRIES, LP - Northfield, Northfield, IL, United States |
| Recall initiated | 2024-03-12 |
| Classified | 2024-05-10 |
| Reported by FDA | 2024-05-22 |
| Distributed | Nationwide (US) |
| Quantity | 50 units |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 10193489069099, 20193489069096 |
| Lot numbers | 0000113381 |
| Model numbers | 91300040 |
Product
Namic FLUID DELIVERY SET, REF 91300040
Reason for recall
Products have a lack of sterility assurance.
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-1807-2024. 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.