🔍 RecallPedia

Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg DOUBLE STRENGTH, 100-count bottle, Rx only, Mfg. by: Mutual Pharmaceutical Company, Inc., Philadelphia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 53489-0146-01

Class I - Dangerous
💊 Drugs Recalled: October 9, 2015 Mutual Pharmaceutical Company Prescription Drugs

What Should You Do?

  1. Check if you have this product:
    Lot # 6727001 Exp 01/18
  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:
Presence of foreign substance -This recall has been intiated due to the presence of a polyethylene piece on the finished product.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg DOUBLE STRENGTH, 100-count bottle, Rx only, Mfg. by: Mutual Pharmaceutical Company, Inc., Philadelphia, PA 19124, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 53489-0146-01

Product Codes/Lot Numbers:

Lot # 6727001 Exp 01/18

Distribution:

Distributed in: MS

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0572-2016

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