FDA Device recall Z-1807-2024
Namic FLUID DELIVERY SET, REF 91300040
- FDA Device
- Class II
- ongoing
- Published 2024-05-22
On 2024-05-22 the FDA classified a Class II recall of Namic FLUID DELIVERY SET, REF 91300040 by Medline Industries Northfield, citing products have a lack of sterility assurance.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1807-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-03-12 |
| Published | 2024-05-22 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
Namic FLUID DELIVERY SET, REF 91300040
Reason
Products have a lack of sterility assurance.
Identifiers
| code_info | UDI/DI 20193489069096 (box), 10193489069099 (unit), Lot Numbers: 0000113381 |
|---|
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-1807-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.