PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: August 9, 2017 Initiated: March 30, 2017 #D-1051-2017

Product Description

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

Reason for Recall

Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.

Details

Units Affected
56,064 36-count cartons
Distribution
Nationwide
Location
Morristown, NJ

Frequently Asked Questions

What product 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. Recalled by Bayer HealthCare Pharmaceuticals, Inc.. Units affected: 56,064 36-count cartons.
Why was this product recalled?
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 9, 2017. Severity: Moderate. Recall number: D-1051-2017.