🔍 RecallPedia

Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.

Class I - Dangerous
🏥 Medical Devices Recalled: December 6, 2018 Vygon U.S.A. Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot codes: 090718FD 250118FD 081117FD 130218FD 050418FD 020518FD
  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:
Vygon U.S.A.
Reason for Recall:
DualStop Caps defect causing leaks in affected product
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Vyon DUALSTOP White Cap used for intravascular lines Product Code: 9888.002- Product Usage: Cap used for intravascular lines.

Product Codes/Lot Numbers:

Lot codes: 090718FD 250118FD 081117FD 130218FD 050418FD 020518FD

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1115-2019

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