Drug recall
AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324
FDA recall event 93147 · Class II · MICROVENTION INC.
Key facts
| Event ID | 93147 |
|---|---|
| Recall numbers | Z-0187-2024 |
| Recalling firm | MICROVENTION INC. |
| Product type | Devices |
| Products | AZUR CX 35 Peripheral Coil System Detachable 13mm x 24 CM, REF: 45-751324 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Peripheral coil system detachable has a potential of unsealed pouch packaging. |
| Initiation date | Aug 24, 2023 |
| Report date | Nov 8, 2023 |
| City | Aliso Viejo |
| State | CA |
| Country | United States |
| FEI number | 3013556777 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: