King Bio Recalls Dr. King's SafeCare Rx Personality Changes Due to Microbial Contamination
King Bio Inc. is recalling 13 bottles of Dr. King's SafeCare Rx Personality Changes 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 recall is classified as FDA Class I, which meets the rubric criteria for a Critical severity score (5).
Plain-English summary
King Bio Inc. is recalling 13 bottles of Dr. King's SafeCare Rx Personality Changes, 2 fl. oz. (59 mL), due to microbial contamination. The affected product is identified by Lot 051716F and an expiration date of 05/19. The product carries NDC 57955-1053-2 and UPC 357955105022.
The recall covers distribution in the United States, Canada, and Australia. The source text does not specify the exact number of units distributed beyond the 13 bottles mentioned in the structured product information, nor does it report any specific illnesses or injuries associated with the contamination.
Consumers who possess 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 may cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's SafeCare Rx Personality Changes, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955105022, NDC 57955-1053-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 13
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: 051716F Exp. 05/19
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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