VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Catalog Number: VIA-27-154-01 UDI: (01)00842429101667(11)190722(17)220630(10)19072208 Lot Number: 19072208
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
MICROVENTION INC.
Reason for Recall:
Due to inadvertently shipping to U.S. customers with international labeling which has some differences with US-cleared labeling.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

VIA Microcatheter VIA 27 REF VIA-27-154-01 - Product Usage: is a single lumen catheter designed to be introduced over a steerable guidewire into the vasculature.

Product Codes/Lot Numbers:

Catalog Number: VIA-27-154-01 UDI: (01)00842429101667(11)190722(17)220630(10)19072208 Lot Number: 19072208

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1830-2021

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