🔍 RecallPedia

CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

Class I - Dangerous
🏥 Medical Devices Recalled: April 26, 2024 Centers For Disease Control and Prevention Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Code: Catalog # FluIVD03-11, lot 220307
  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:
Centers For Disease Control and Prevention
Reason for Recall:
The H5b component may fail to amplify, resulting in an inconclusive result.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

CDC, Influenza A/H5 Subtyping Kit, Model/Catalog Number: FluIVD03-11

Product Codes/Lot Numbers:

Lot Code: Catalog # FluIVD03-11, lot 220307

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2220-2024