Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1828-2021 — VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

U.S. FDA — Device Enforcement · United States · 2021-04-21 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1828-2021
Date of alert: 2021-04-21
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: MICROVENTION INC.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00842429101643

Reported risk: Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-1828-2021 — VIA Microcatheter VIA 17 REF VIA-17-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

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