FDA Recalls King Bio Homeopathic Muscle Maximizer Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Muscle Maximizer 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 source text explicitly identifies the recall as FDA Class I, which corresponds to a Critical severity score of 5 according to the rubric.
Plain-English summary
The U.S. Food and Drug Administration (FDA) has issued a Class I recall for Dr. King's Natural Medicine Homeopathic Muscle Maximizer, 2 fl. oz. (59 mL), manufactured by King Bio Inc. The recall is due to microbial contamination. The affected product is identified by NDC 57955-5133-2 and UPC 357955513322.
The recall involves 291 bottles with the following lot numbers and expiration dates: 010118AE (Exp. 01/20), 050216L (Exp. 05/2019), and 092216E (Exp. 09/2019). The product was distributed nationwide in the United States, as well as in Canada and Australia.
Consumers who have this product should stop using it and contact King Bio Inc. for further instructions or a refund. The FDA classifies this as a Class I recall, which is the most serious type of recall, indicating a reasonable probability that the use of or exposure to the violative product will cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Muscle Maximizer, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955513322, NDC 57955-5133-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 291
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 (3)
- Lot Numbers: 010118AE Exp. 01/20
- 050216L Exp. 05/2019
- 092216E Exp. 09/2019
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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