The Recall Desk
CriticalFDA (Drugs)·D-0585-2019·Announced 2019-03-20

King Bio Homeopathic Grains & Gluten Intolerances Recalled for Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Grains & Gluten Intolerances 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 agency classification is FDA Class I, which mandates a minimum severity score of 5 according to the rubric.

Plain-English summary

King Bio Inc. is recalling 360 bottles of Dr. King's Natural Medicine Homeopathic Grains & Gluten Intolerances, 2 fl. oz. (59 mL). The recall was initiated due to microbial contamination. The product is identified by NDC 57955-0724-2 and UPC 357955520429.

The affected lots include 012517G (Exp. 01/20), 040716A (Exp. 04/19), and 052516Z (Exp. 05/19). 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.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Grains & Gluten Intolerances, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955520429, NDC 57955-0724-2
Manufacturer
King Bio Inc.
Affected units
360

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: 012517G Exp. 01/20
  • 040716A Exp. 04/19
  • 052516Z 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 →