🔍 RecallPedia

Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500044048

Class I - Dangerous
💊 Drugs Recalled: March 30, 2017 Bayer HealthCare Pharmaceuticals Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    BTAHDG0; Exp. 04/19
  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:
Bayer HealthCare Pharmaceuticals, Inc.
Reason for Recall:
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 24-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500044048

Product Codes/Lot Numbers:

BTAHDG0; Exp. 04/19

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1050-2017

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