The Recall Desk
CriticalFDA (Drugs)·D-0966-2019·Announced 2019-03-20

King Bio Recalls Regional Allergies Canadian Prairies Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Regional Allergies Canadian Prairies 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 per the rubric mandates a severity score of 5 (Critical).

Plain-English summary

King Bio Inc. is recalling 710 bottles of Dr. King's Natural Medicine Regional Allergies Canadian Prairies, 59 mL (liquid/liquide). The recall is due to microbial contamination. The affected product has the Lot number 021517L and an expiration date of 02/20.

The product was distributed nationwide in the United States, as well as in Canada and Australia. The FDA has classified this recall as Class I, which indicates a reasonable probability that use of or exposure to the violative 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 Regional Allergies Canadian Prairies, 59 mL (liquid/liquide), DIN-HM 80074815 UPC 357955181729
Manufacturer
King Bio Inc.
Affected units
710

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 (1)

  • Lot: 021517L 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 →