HelloLife Recalls Thyroveev Homeopathic Medicine Due to Microbial Contamination
HelloLife is recalling 370 bottles of Thyroveev homeopathic medicine due to microbial contamination. The product was distributed nationwide and internationally.
The agency’s classification
FDA (Drugs): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
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 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The FDA has classified this recall as Class I, which meets the rubric criteria for a Critical severity score (5).
Plain-English summary
HelloLife, Inc. is recalling 370 bottles of Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle. The recall is due to microbial contamination, specifically the presence of microorganisms including Staphylococcus saprophyticus and Burkholderia cepacia. The affected product is identified by Lot TV/030717F and has an expiration date of 7/2019.
The recalled product was distributed nationwide in the United States and in numerous international locations, including Canada, the United Kingdom, and various countries in Europe, Asia, and the Americas. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product will cause serious adverse health consequences or death.
Consumers who have purchased this product should stop using it immediately and contact HelloLife, Inc. for instructions on how to return the product or obtain a refund. The manufacturer is located at 4635 40th St SE, Grand Rapids, MI 49512.
The recalled product
- Product
- Thyroveev, Homeopathic (OTC Medicine), 2 fl oz (59 mL) per bottle, Mftd for: HelloLife, Inc. 4635 40th St SE, Grand Rapids, MI 49512. NDC: 49726-025-02
- Manufacturer
- Hellolife
- Category
- Drug — OTC Medicine
- Affected units
- 370
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)
- Lot: TV/030717F
- exp 7/2019
Distribution
Part of a larger recall action
This product is one of 4 recalled by Hellolife 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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