FDA Recalls King Bio Homeopathic Snore Control for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Snore Control due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
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 classified this recall as Class I, which corresponds to a reasonable probability that use of the product could cause serious adverse health consequences or death.
Plain-English summary
King Bio Inc. is voluntarily recalling 14,781 bottles of Dr. King's Natural Medicine Homeopathic Snore Control, 2 fl. oz. (59 mL). The recall was initiated because the product was found to be contaminated with microbes.
The affected product is identified by NDC 57955-5120-2 and UPC 357955512028. Specific lot numbers and expiration dates are listed in the recall notice, including lots expiring in 2018, 2019, and 2020. The product was distributed nationwide in the United States, as well as in Canada and Australia.
Consumers who have purchased this product should stop using it and return it to the place of purchase for a refund or contact the manufacturer for further instructions. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product could cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Snore Control, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512028, NDC 57955-5120-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 14,781
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 (9)
- Lots: 052516Y Exp. 05/19
- 060518C Exp. 06/20
- 060917F Exp. 06/19
- 070518A Exp. 07/20
- 080317C Exp. 08/19
- 081015B Exp. 08/18
- 081815G Exp. 08/18
- 111516C Exp. 11/19
- 112317E 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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