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Home > Recalled Products > Drugs > Lack of Proper Labeling > Bayer Alka-Seltzer Plus

Recall: Bayer Alka-Seltzer Plus


On 2018-03-15, the FDA announced that Bayer is conducting a recall on Alka-Seltzer Plus due to a possible lack of proper labeling. The recalled products were sold under the brand name(s) Bayer during an unspecified time period throughout the regions shown in the map below.

In recent months, there have been 1 drugs recalls due to potential lack of proper labeling, including amitriptyline hcl and phenobarbital tablets, lamotrigine and more. Additionally, there have been 21 drug and medical device recalls due to other health hazards as well as 82 food recalls.

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Product Image of Alka-Seltzer Plus included in recall with Bayer Logo with Green background
Note: Images may not be available for every version. Please review the detailed description below.

Company Contact Information:

Name: Bayer
Phone: 1-800-986-0369

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Detailed Recall Information

Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.

Product Description: Alka-Seltzer Plus

Brand Name(s): Bayer

Reason for Recall: Lack of Proper Labeling

Official Recall Date: 2018-03-15


Additional information provided by the

Bayer is voluntarily recalling Alka-Seltzer Plus packages that: Read More.

More information may be available at

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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.

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