The Recall Desk
CriticalFDA (Drugs)·D-0610-2019·Announced 2019-03-20

King Bio Homeopathic Grief & Guilt Reliever Recalled for Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Grief & Guilt Reliever 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 meets the rubric criteria for a Critical severity score (5).

Plain-English summary

King Bio Inc. is recalling 400 bottles of Dr. King's Natural Medicine Homeopathic Grief & Guilt Reliever, 2 fl. oz. (59 mL). The recall is due to microbial contamination. The affected product is identified by NDC 57955-5038-2 and UPC 357955503828.

The recalled lots are 022417G (Exp. 02/20), 052516N (Exp. 05/19), and 080416D (Exp. 08/19). 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. The FDA has classified this recall as Class I, indicating a reasonable probability that use of the product may cause serious adverse health consequences or death.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Grief & Guilt Reliever, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955503828, NDC 57955-5038-2
Manufacturer
King Bio Inc.
Affected units
400

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)

  • Lots: 022417G Exp. 02/20
  • 052516N Exp. 05/19
  • 080416D Exp. 08/19

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 →