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.
Company Contact Information:
Do you work for a company involved with this recall? Contact us to learn how you can control data, information and ads shown on this page.
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 FDA.gov:
Bayer is voluntarily recalling Alka-Seltzer Plus packages that: Read More.
More information may be available at FDA.gov
Latest Safety Recalls
Select image for details, including additional styles.
Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.