King Bio Recalls Homeopathic Morning Sickness Relief Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Morning Sickness Relief 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 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The agency classification is FDA Class I, which mandates a minimum severity score of 4 per the rubric. Microbial contamination in a drug product represents a significant health risk.
Plain-English summary
King Bio Inc. is recalling 452 bottles of Dr. King's Natural Medicine Homeopathic Morning Sickness Relief, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The affected product has NDC 57955-6008-2 and UPC 357955500827.
The recalled product was distributed nationwide in the U.S., as well as in Canada and Australia. Specific lot numbers include 040616K (Exp. 04/2019) and 072716J (Exp. 07/2019).
Consumers should check their inventory for these specific lot numbers and expiration dates. If they possess the affected product, they should stop using it and contact the manufacturer for instructions on disposal or return.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Morning Sickness Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955500827, NDC 57955-6008-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 452
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 Numbers: 040616K Exp. 04/2019
- 072716J Exp. 07/2019
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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