ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.

Class I - Dangerous
💊 Drugs Recalled: May 31, 2019 Chiesi USA Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lots: 3171855, Exp. 12/19
  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:
Chiesi USA, Inc.
Reason for Recall:
Failed Dissolution Specifications: Out of specification result for dissolution.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

ZYFLO CR (zileuton) extended-release tablets, 600 mg, 120-count bottles, Rx only, Distributed by Chiesi USA, Inc., Cary, NC 27518, NDC 10122-902-12.

Product Codes/Lot Numbers:

Lots: 3171855, Exp. 12/19

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1341-2019

Related Recalls