FDA Announces Nationwide Voluntary Recall of Hyland’s Teething Tablets

FDA has announced a nationwide voluntary recall of all lots of Hyland’s Baby Teething Tablets and Hyland’s Baby Nighttime Teething Tablets from Standard Homeopathic Company.

Standard Homeopathic Company is notifying its distributors and retailers by mail and is arranging for the return of all recalled products.  Consumers who have products which are being recalled should contact the company.

Consumers with questions regarding this recall can contact Standard Homeopathic Company by calling 1-800-991-3376. Consumers should contact their physician or healthcare provider if they believe they have experienced any problems that may be related to the product.

FDA reminds consumers that homeopathic teething tablets containing belladonna pose an unnecessary risk to infants and children and urges consumers not to use these products.

In January 2017, the FDA announced its laboratory analysis had found inconsistent amounts of belladonna, a toxic substance, in certain homeopathic teething tablets including Hyland’s. The FDA contacted Standard Homeopathic Company on January 25 regarding a recall of its homeopathic teething tablet products labeled as containing belladonna, in order to protect consumers from inconsistent levels of belladonna.