Bayer Recalls Alka-Seltzer Extra Strength Tablets Due to Defective Packaging
Bayer is recalling Alka-Seltzer Extra Strength effervescent tablets because customer complaints confirmed small holes or cracks in the foil blister packs.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard is a packaging defect (holes/cracks in foil) without reported injuries or illnesses, fitting the criteria for moderate severity.
Plain-English summary
Bayer HealthCare Pharmaceuticals, Inc. is recalling 24,672 cartons of Alka-Seltzer Extra Strength effervescent tablets. The product is distributed nationwide and is identified by the code BTAHDG0 and expiration date 04/19.
The recall was initiated due to a defective container issue. Customer complaints confirmed the presence of small holes or cracks in the foil of the blister packs. This defect could potentially compromise the integrity of the packaging.
Consumers who have this product should stop using it and contact Bayer HealthCare for a refund or replacement. The recall is classified as Class II by the FDA.
The recalled product
- Product
- 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
- Manufacturer
- Bayer HealthCare Pharmaceuticals, Inc.
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- BTAHDG0
- Exp. 04/19
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 3 recalled by Bayer HealthCare Pharmaceuticals, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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