The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0623-2019·Announced 2019-03-20

FDA Recalls King Bio Homeopathic ClaustroPlex Due to Microbial Contamination

King Bio Inc. is recalling 34 bottles of Dr. King's Natural Medicine Homeopathic ClaustroPlex due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

The agency’s classification

FDA (Drugs): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 4/5 (Severe).

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

Our severity reasoning: The agency classification is FDA Class I, which mandates a severity score of at least 4 per the rubric. The hazard involves microbial contamination, a significant health risk.

Plain-English summary

King Bio Inc. is recalling 34 bottles of Dr. King's Natural Medicine Homeopathic ClaustroPlex, 2 fl. oz. (59 mL). The recall was initiated due to microbial contamination. The affected product is identified by NDC 57955-5035-2 and UPC 357955503521.

The recalled product was distributed nationwide in the United States, as well as in Canada and Australia. The specific lots affected are 021016J (Expiration 02/19) and 063016H (Expiration 06/19).

Consumers should check their inventory for these specific lot numbers and expiration dates. If they possess the affected product, they should stop using it and contact King Bio Inc. for further instructions.

The recalled product

Product
Dr. King's Natural Medicine Homeopathic ClaustroPlex, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806, UPC 357955503521, NDC 57955-5035-2
Manufacturer
King Bio Inc.
Category
Drug — Homeopathic
Hazard
Affected units
34

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 (2)

  • Lots: 021016J Exp. 02/19
  • 063016H 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 →

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