FDA Recalls King Bio Hemorrhoid Relief Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Hemorrhoid Relief 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 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. 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 or exposure to the violative 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 Dr. King's Natural Medicine Homeopathic Hemorrhoid Relief, 2 fl. oz. (59 mL), due to microbial contamination. The recall involves 2,045 bottles of the product.
The affected product is identified by NDC 57955-5023-2 and UPC 357955502326. Specific lot numbers and expiration dates include 012317C (Exp. 01/20), 052516U (Exp. 05/19), and 050216S (Exp. 05/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.
Consumers should check their inventory for these specific lot numbers and expiration dates. If the product is found, it should be returned to the place of purchase or disposed of according to local regulations.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Hemorrhoid Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955502326, NDC 57955-5023-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 2,045
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)
- Lot Numbers: 012317C Exp. 01/20
- 052516U Exp. 05/19
- 050216S 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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