Bayer HealthCare Pharmaceuticals, Inc. recalls Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbon…
- Recall date
- March 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1051-2017
- FDA classification
- Class II
- Brand / firm
- Bayer HealthCare Pharmaceuticals, Inc.
- Sold / distributed
- Nationwide
Why it was recalled
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Alka-Seltzer Gold (1000 mg Anhydrous citric acid, 344 mg Antacid Potassium bicarbonate, 1050 mg Antacid Sodium bicarbonate/Antacid) Effervescent Tablets, 36-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500041085
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