🔍 RecallPedia

Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01

Class I - Dangerous
💊 Drugs Recalled: July 16, 2015 Mutual Pharmaceutical Company Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    lot #s: 6667301 & 6667401, exp 11/15 and 6699201, exp 6/16
  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:
Mutual Pharmaceutical Company, Inc.
Reason for Recall:
Chemical Contamination; benzophenone leached from the product label varnish
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01

Product Codes/Lot Numbers:

lot #s: 6667301 & 6667401, exp 11/15 and 6699201, exp 6/16

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1422-2015

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