The Recall Desk
SevereFDA (Drugs)·D-0571-2019·Announced 2019-03-20

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.

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 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.
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.

See all 465 products in this recall →