Drug recall
ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy…
FDA recall event 95151 · Class II · MICROVENTION INC.
Key facts
| Event ID | 95151 |
|---|---|
| Recall numbers | Z-3157-2024 |
| Recalling firm | MICROVENTION INC. |
| Product type | Devices |
| Products | ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device designed to restore blood flow by effectively removing clots from occlusive… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to Retrieval Device product labels stating the incorrect expiration dates that (5 years instead of 3 years) which extends beyond their true expiration date. |
| Initiation date | Aug 5, 2024 |
| Report date | Sep 25, 2024 |
| 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: