The Recall Desk
SevereFDA (Drugs)·D-0523-2019·Announced 2019-03-20

FDA Recalls King Bio Homeopathic Male Libido Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Male Libido 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 696 bottles of Dr. King's Natural Medicine Homeopathic Male Libido, 2 fl. oz. (59 mL), due to microbial contamination. The product is identified by NDC 57955-5510-2 and UPC 3579555101022.

The affected lots include 030216F (Exp. 03/19), 051216K (Exp. 05/19), 080315E (Exp. 08/2018), 080916Q (Exp. 08/2019), and 120816E (Exp. 12/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers should stop using the product and return it to the place of purchase for a refund or contact the manufacturer for further instructions.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Male Libido, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 3579555101022, NDC 57955-5510-2
Manufacturer
King Bio Inc.
Affected units
696

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 (5)

  • Lot Numbers: 030216F Exp. 03/19
  • 051216K Exp. 05/19
  • 080315E Exp. 08/2018
  • 080916Q Exp. 08/2019
  • 120816E Exp. 12/19

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 →