Reumofan Plus Tablets, 30-count bottle per Box, (remaining label information in Spanish)

Class I - Dangerous
💊 Drugs Recalled: August 27, 2012 Samantha Lynn Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    all lots within expiry through 2016
  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:
Samantha Lynn, Inc
Reason for Recall:
Marketed without an approved NDA/ANDA: Samantha Lynn Inc. is recalling Reumofan Plus Tablets because it contains undeclared drug ingredients making it an unapproved drug.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Reumofan Plus Tablets, 30-count bottle per Box, (remaining label information in Spanish)

Product Codes/Lot Numbers:

all lots within expiry through 2016

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-063-2013