FDA Device recall Z-0002-2020
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture…
- FDA Device
- Class II
- ongoing
- Published 2019-10-09
On 2019-10-09 the FDA classified a Class II recall of SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture… by The Metrix, citing potential for leaking product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0002-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2018-09-21 |
| Published | 2019-10-09 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | The Metrix |
| Distribution | US |
Product
SECURE EVA - DUAL CHAMBER CONTAINER With Screw Connectors, 3000mL, (legless) REF 66630 - Product Usage: For use in an intravenous admixture program. The empty container will be filled with parenteral admixtures under normal pharmacy conditions, e.g. laminar flow hood. The use of this product is for storage and delivery of intravenous parenteral admixtures.
Reason
Potential for leaking product
Identifiers
| code_info | Lot Numbers: 66630-A2771, 66630-A4282 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0002-2020%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.