MICROVENTION INC. Recall 88024
Description: VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.
MICROVENTION INC. Recall 88024 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1829-2021 |
| Event ID | 88024 |
| Event Description | VIA Microcatheter VIA 21 REF VIA-21-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature. |
| Product Type | Devices |
| Distribution | U.S. Nationwide distribution in the states of FL, IA, MI, MN, TN and TX. |
| Recall Reason | Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling. |
| Device Classification | 20210616 |
| Device Code Info | Catalog Number: VIA-21-154-01 UDI: (01)00842429101650(11)191104(17)221031(10)19110403M Lot Number: 19110403M |
| Center Classification Date | 20210607 |
| Recall Initiation Date | 20210421 |
| Recalling Firm | MICROVENTION INC. |
| Initial Notification | Letter |
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