VIA Microcatheter VIA 21 REF VIA-21-154-01 — Class III medical device recall Z-1829-2021
Terminated recall by MICROVENTION INC., reported 2021-06-16, distributed nationwide. Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US
| Recall number | Z-1829-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MICROVENTION INC., Aliso Viejo, CA, United States |
| Recall initiated | 2021-04-21 |
| Classified | 2021-06-07 |
| Reported by FDA | 2021-06-16 |
| Terminated | 2024-02-16 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00842429101650 |
| Lot numbers | 19110403M |
| Model numbers | VIA-21-154-01 |
Product
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.
Reason for recall
Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1829-2021. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.