King Bio Recalls Dr. King's SafeCare Rx SYP Miasm Constitution Due to Microbial Contamination
King Bio Inc. is recalling 85 bottles of Dr. King's SafeCare Rx SYP Miasm Constitution 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 source metadata explicitly identifies the agency classification as Class I, which corresponds to a Critical severity score of 5 according to the rubric.
Plain-English summary
King Bio Inc. is recalling 85 bottles of Dr. King's SafeCare Rx SYP Miasm Constitution, 2 fl. oz. (59 mL), due to microbial contamination. The product is identified by NDC 57955-0306-2 and UPC 357955030324.
The recall covers two specific lots: Lot 012517H with an expiration date of 01/20, and Lot 081015N with an expiration date of 08/18. The affected units were distributed nationwide in the United States, as well as in Canada and Australia.
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 may cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's SafeCare Rx SYP Miasm Constitution, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955030324, NDC 57955-0306-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 85
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: 012517H Exp. 01/20
- 081015N Exp. 08/18
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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