King Bio Recalls Homeopathic Adrenal Burnout Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Adrenal Burnout due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
What this means for you
Highest-severity recall. Risk of serious injury or death is documented or strongly suspected. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The FDA has classified this recall as Class I, which meets the rubric criteria for a Critical severity score (5).
Plain-English summary
King Bio Inc. is recalling 4,888 bottles of Dr. King's Natural Medicine Homeopathic Adrenal Burnout, 2 fl. oz. (59 mL). The recall is being conducted due to microbial contamination. The affected product is identified by NDC 57955-1434-2 and UPC 357955597926.
The recalled product was distributed nationwide in the United States, as well as in Canada and Australia. Specific lots affected include 050218E (Exp. 05/20), 080317E (Exp. 08/19), 120216A (Exp. 12/19), and 120217F (Exp. 12/19).
Consumers who have purchased this product should stop using it and contact King Bio Inc. for further instructions or a refund. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product will cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Adrenal Burnout, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955597926, NDC 57955-1434-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 4,888
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 (4)
- Lots: 050218E Exp. 05/20
- 080317E Exp. 08/19
- 120216A Exp. 12/19
- 120217F Exp. 12/19
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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