King Bio Recalls UlcerPlex Detox Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic UlcerPlex Detox 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 severity score of at least 4 per the rubric.
Plain-English summary
King Bio Inc. is recalling 90 bottles of Dr. King's Natural Medicine Homeopathic UlcerPlex Detox, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The affected product is identified by NDC 57955-5074-2 and UPC 357955507420.
The recalled lots are 051716D (Exp. 05/19) and 100316H (Exp. 10/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.
Consumers should stop using the product and contact King Bio Inc. for instructions on disposal or return.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic UlcerPlex Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955507420, NDC 57955-5074-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 90
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)
- Lots: 051716D Exp. 05/19
- 100316H Exp. 10/19
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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