FDA Device recall Z-0333-2025
CORMIX 250 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64045
- FDA Device
- Class II
- ongoing
- Published 2024-11-20
On 2024-11-20 the FDA classified a Class II recall of CORMIX 250 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64045 by The Metrix, citing A limited number of IV bags have been found to leak during filling.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0333-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-10-09 |
| Published | 2024-11-20 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | The Metrix |
| Distribution | US |
Product
CORMIX 250 mL EMPTY EVA CONTAINER With 2 Ports, REF MS64045; An empty single-use pouch made of plastic intended to contain a fluid for intravenous (IV) administration.
Reason
A limited number of IV bags have been found to leak during filling.
Identifiers
| code_info | UDI/DI 00812496011121, Lot Numbers: 64045-A8305, 64045-A8341, 64045-A8366, 64045-A8377, 64045-A8405, 64045-A8411, 64045-A8447, 64045-A8469, 64045-A8485 |
|---|
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-0333-2025%22
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