The Recall Desk
CriticalFDA (Drugs)·D-0642-2019·Announced 2019-03-20

King Bio Recalls Homeopathic Jet Lag Product Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change 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 recall is classified as FDA Class I, which meets the rubric criteria for a Critical severity score (5).

Plain-English summary

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change, 2 fl. oz. (59 mL), due to microbial contamination. The recall involves 377 bottles of the product, identified by Lot 060216D with an expiration date of 06/19. The product is manufactured by King Bio Inc. and carries NDC 57955-5126-2 and UPC 357955512622.

The affected product was distributed nationwide in the United States, as well as in Canada and Australia. The U.S. Food and Drug Administration 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 check their lot numbers and expiration dates. If the product matches the recalled lot, consumers should stop using it and contact the manufacturer for further instructions or a refund.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512622, NDC 57955-5126-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic Medicine
Hazard
Affected units
377

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)

  • Lots: 060216D Exp. 06/19

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.

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Same hazard · microbial contamination

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