The Recall Desk
CriticalFDA (Drugs)·D-0964-2019·Announced 2019-03-20

King Bio Inc. Recalls Regional Allergies Liquid Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Regional Allergies Eastern Canada liquid 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 FDA has classified this recall as Class I, which corresponds to a Critical severity score of 5 according to the rubric.

Plain-English summary

King Bio Inc. is recalling Dr. King's Natural Medicine Regional Allergies Eastern Canada, 59 mL liquid, due to microbial contamination. The recall involves 957 bottles with lot numbers 060917E (Exp. 06/20) and 021517K (Exp. 02/20). The product is identified by DIN-HM 80075212 and UPC 357955181620.

The affected product was 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 or exposure to the violative product will cause serious adverse health consequences or death.

Consumers who have purchased this product should stop using it and contact King Bio Inc. for further instructions or a refund. The specific microbial agent was not identified in the provided source text.

The recalled product

Product
Dr. King's Natural Medicine Regional Allergies Eastern Canada, 59 mL, (liquid/liquide) DIN-HM 80075212 UPC 357955181620
Manufacturer
King Bio Inc.
Affected units
957

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: 060917E Exp. 06/20
  • 021517K Exp. 02/20

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 →