King Bio Aquaflora Heavy Metal Detox Recalled for Microbial Contamination
King Bio Inc. is recalling Aquaflora Heavy Metal Detox Candida 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 has classified this recall as Class I, which per the rubric mandates a severity score of 5 (Critical) regardless of other factors.
Plain-English summary
King Bio Inc. is recalling Aquaflora Heavy Metal Detox Candida, a 2 fl. oz. homeopathic product, due to microbial contamination. The recall involves 2,086 bottles with Lot 080216A and an expiration date of 08/19.
The product was distributed nationwide in the United States, as well as in Canada and Australia. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product may cause serious adverse health consequences or death.
Consumers who have purchased this product should stop using it and contact King Bio Inc. for further instructions or a refund.
The recalled product
- Product
- Aquaflora Heavy Metal Detox Candida, 2 fl. oz. (59 mL), Homeopathic, King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, NDC 57955-2281-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 2,086
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 (1)
- Lot: 080216A Exp. 08/19
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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