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
Reported: August 9, 2017 Initiated: March 30, 2017 #D-1050-2017
Product 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
Reason for Recall
Defective Container: Confirmed customer compliant of small holes or cracks in the foil of blister packs.
Details
- Recalling Firm
- Bayer HealthCare Pharmaceuticals, Inc.
- Units Affected
- 24,672 24-count cartons
- Distribution
- Nationwide
- Location
- Morristown, NJ
Frequently Asked Questions
What product 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. Recalled by Bayer HealthCare Pharmaceuticals, Inc.. Units affected: 24,672 24-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-1050-2017.
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