King Bio Recalls Kids Multi-Strain Flu Relief Homeopathic for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Kids Multi-Strain Flu Relief Homeopathic due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that use of the product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a score of 4 or higher.
Plain-English summary
King Bio Inc. is recalling 3,271 bottles of Dr. King's Natural Medicine Kids Multi-Strain Flu Relief Homeopathic, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The affected product has the NDC 57955-0422-2 and UPC 357955042228.
The recalled lots are 071316A (Exp. 07/2019), 111015B (Exp. 11/2018), and 112015A (Exp. 11/2018). The product was distributed nationwide in the U.S.A., as well as in Canada and Australia.
Consumers should check their home medicine cabinets for this specific product and lot numbers. If found, they should stop using the product and contact King Bio Inc. for further instructions or a refund.
The recalled product
- Product
- Dr. King's Natural Medicine Kids Multi-Strain Flu Relief Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside dr. Asheville, NC 28806 USA, UPC 357955042228, NDC 57955-0422-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 3,271
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)
- Lots: 071316A Exp. 07/2019
- 111015B Exp. 11/2018
- 112015A Exp. 11/2018
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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