Bayer HealthCare Pharmaceuticals, Inc. recalls Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID), 1985 mg Analgesic Sodium bicarbonate/Antacid, 1000 mg Anhydrous Ci…
- Recall date
- March 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-1050-2017
- 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 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
Get recall alerts
Free email alert whenever Bayer HealthCare Pharmaceuticals, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Bayer HealthCare Pharmaceuticals, Inc.