The Recall Desk
SevereFDA (Drugs)·D-0543-2019·Announced 2019-03-20

FDA Recalls Homeopathic Restless Leg Symptom Relief Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Restless Leg Symptom Relief 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 or exposure to the violative product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a severity score of 4 or higher.

Plain-English summary

King Bio Inc. is recalling 5,080 bottles of Dr. King's Natural Medicine Homeopathic Restless Leg Symptom Relief, 2 fl. oz. (59 mL). The recall was initiated because the product is subject to microbial contamination.

The affected product is identified by NDC 57955-6235-2 and UPC 357955544524. Specific lot numbers and expiration dates include 031218D (Exp. 03/20), 042717C (Exp. 04/20), 072815A (Exp. 07/18), 092216C (Exp. 09/19), and 120217E (Exp. 12/19). The product was distributed nationwide in the United States, as well as in Canada and Australia.

Consumers who have purchased this product should check their lot numbers and expiration dates against the list above. If the product matches the recalled items, consumers should stop using it and contact the manufacturer for further instructions.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic Restless Leg Symptom Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955544524, NDC 57955-6235-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic Medicine
Hazard
Affected units
5,080

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: 031218D Exp. 03/20
  • 042717C Exp. 04/20
  • 072815A Exp. 07/18
  • 092216C Exp. 09/19
  • 120217E 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 →

Related recalls

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Same hazard · microbial contamination

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