The Recall Desk
Agency classClass IOur severity:CriticalFDA (Drugs)·D-0625-2019·Announced 2019-03-20

King Bio Recalls Homeopathic Better Breath Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Better Breath due to microbial contamination. The affected 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 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The FDA has classified this recall as Class I, which meets the rubric criteria for a Critical severity score (5).

Plain-English summary

King Bio Inc. is recalling 17 bottles of Dr. King's Natural Medicine Homeopathic Better Breath, 2 fl. oz. (59 mL), due to microbial contamination. The product is identified by UPC 357955880127 and includes lots 010118F (Exp. 01/20) and 051716E (Exp. 05/19).

The recall covers product distributed nationwide in the United States, as well as in Canada and Australia. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product will cause serious adverse health consequences or death.

Consumers who have 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 Better Breath, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955880127
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic Medicine
Hazard
Affected units
17

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 (2)

  • Lots: 010118F Exp. 01/20
  • 051716E 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 →

Related recalls

Same manufacturer · King Bio Inc.

See all →

Same hazard · microbial contamination

See all →

Similar recalls