King Bio Recalls Homeopathic Stress Control Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Stress Control due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that use of the product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a score of 4 or higher.
Plain-English summary
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Stress Control, 2 fl. oz. (59 mL), due to microbial contamination. The recall involves 5,170 bottles with specific lot numbers and expiration dates.
The affected product was distributed nationwide in the United States, as well as in Canada and Australia. The specific lot numbers are 012616B (Exp. 01/19), 020817E (Exp. 02/20), 071818G (Exp. 07/20), and 111017C (Exp. 11/19).
Consumers should check their inventory for these specific lot numbers and expiration dates. If they possess the recalled product, they should stop using it and contact King Bio Inc. for further instructions.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Stress Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507925, NDC 57955-5852-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 5,170
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 (4)
- Lot Numbers: 012616B Exp. 01/19
- 020817E Exp. 02/20
- 071818G Exp. 07/20
- 111017C Exp. 11/19
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 465 recalled by King Bio 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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