FDA Device recall Z-1429-2025
namic convenience kits labeled as: KIT,ARTERIAL,60,(152CM),PG
- FDA Device
- Class II
- ongoing
- Published 2025-04-02
On 2025-04-02 the FDA classified a Class II recall of namic convenience kits labeled as: KIT,ARTERIAL,60,(152CM),PG by Medline Industries Northfield, citing the female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1429-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-02-12 |
| Published | 2025-04-02 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Medline Industries Northfield |
| Distribution | US |
Product
namic convenience kits labeled as: KIT,ARTERIAL,60,(152CM),PG; medical convenience kit, REF 70036160
Reason
The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.
Identifiers
| code_info | UDI/DI 10193489064803 (each), 20193489064800 (case), Lot number 0000140054 |
|---|
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-1429-2025%22
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