King Bio Homeopathic Flu Relief Recalled for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Multi-Strain Flu Relief 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 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 Dr. King's Natural Medicine Homeopathic Multi-Strain Flu Relief, 2 fl. oz. (59 mL), due to microbial contamination. The recall involves 10,025 bottles of the product, identified by NDC 57955-5194-2 and UPC 357955519928.
The affected lots include 013018A (Exp. 01/2020), 020618B (Exp. 02/20), 072716H (Exp. 07/19), and 120617A (Exp. 12/2019). The product was distributed nationwide in the United States, as well as in Canada and Australia.
Consumers should stop using the product and contact King Bio Inc. for further instructions or a refund. This recall is classified as Class I by the FDA, indicating a reasonable probability that use of the product may cause serious adverse health consequences or death.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Multi-Strain Flu Relief, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955519928, NDC 57955-5194-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 10,025
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: 013018A Exp. 01/2020
- 020618B Exp. 02/20
- 072716H Exp. 07/19
- 120617A Exp. 12/2019
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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