The Recall Desk
SevereFDA (Drugs)·D-0561-2019·Announced 2019-03-20

King Bio Homeopathic Urinary Tract Irritations Recalled for Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Urinary Tract Irritations 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 agency classification is FDA Class I, which mandates a severity score of at least 4 according to the rubric.

Plain-English summary

King Bio Inc. is recalling 1,443 bottles of Dr. King's Natural Medicine Homeopathic Urinary Tract Irritations, 2 fl. oz. (59 mL). The recall was initiated because the product is subject to microbial contamination.

The affected product is identified by NDC 57955-5062-2 and UPC 357955505228. Specific lot numbers and expiration dates include 033116K (Exp. 03/19), 060616A (Exp. 06/19), 071316L (Exp. 07/19), 080315G (Exp. 08/18), and 111516D (Exp. 11/19). The product was 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 recalled product

Product
Dr. King's Natural Medicine Homeopathic Urinary Tract Irritations, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955505228, NDC 57955-5062-2
Manufacturer
King Bio Inc.
Affected units
1,443

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 (5)

  • Lot Numbers: 033116K Exp. 03/19
  • 060616A Exp. 06/19
  • 071316L Exp. 07/19
  • 080315G Exp. 08/18
  • 111516D Exp. 11/19

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 →