Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.

Class I - Dangerous
🏥 Medical Devices Recalled: November 12, 2024 Aerin Medical Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #10235, exp. 2026-05-01; UDI (01)08886479300269(17)260501(10)10235
  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:
Aerin Medical, Inc.
Reason for Recall:
Some units in a single production lot were programmed incorrectly which will result in the VivAer Stylus being incorrectly recognized as RhinAer Stylus when connected to the Aerin Console.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Aerin Medical VivAer Stylus, REF CAT1785 (individual stylus), and REF CAT500 (5-pack), sterile.

Product Codes/Lot Numbers:

Lot #10235, exp. 2026-05-01; UDI (01)08886479300269(17)260501(10)10235

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0808-2025