The Recall Desk
SevereFDA (Drugs)·D-0638-2019·Announced 2019-03-20

King Bio Homeopathic Fears & Nightmares Recalled for Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Fears & Nightmares due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

What this means for you

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that use of the product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a score of 4 or higher.

Plain-English summary

King Bio Inc. is recalling 275 bottles of Dr. King's Natural Medicine Homeopathic Fears & Nightmares, 2 fl. oz. (59 mL). The recall was initiated because the product was found to be microbially contaminated.

The affected product is identified by NDC 57955-5099-2 and UPC 357955509929. Specific lots involved include 052616F (Exp. 05/19), 063015C (Exp. 06/18), and 102816K (Exp. 10/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers who have purchased 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 Fears & Nightmares, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955509929, NDC 57955-5099-2
Manufacturer
King Bio Inc.
Affected units
275

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: 052616F Exp. 05/19
  • 063015C Exp. 06/18
  • 102816K Exp. 10/19

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 →