The Recall Desk
Agency classClass IOur severity:SevereFDA (Drugs)·D-0694-2019·Announced 2019-03-20

FDA Recalls King Bio Psoriasis Lotion Due to Microbial Contamination

King Bio Inc. is recalling Dr. King's Natural Medicine Psoriasis Symptom Relief Homeopathic Topical Lotion 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 minimum severity score of 4 per the rubric. The hazard involves microbial contamination, a significant health risk.

Plain-English summary

King Bio Inc. is recalling Dr. King's Natural Medicine Psoriasis Symptom Relief Homeopathic Topical Lotion, 3 oz. (85 g), due to microbial contamination. The recall involves 1,732 tubes of the product.

The affected product is identified by NDC 57955-0920-3 and UPC 357955092032. Specific lots include 013018ZZ (Exp. 01/20), 021217ZZ (Exp. 02/19), and 110717ZZ (Exp. 11/19). The product was distributed nationwide in the U.S.A., as well as in Canada and Australia.

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

The recalled product

Product
Dr. King's Natural Medicine Psoriasis Symptom Relief Homeopathic Topical Lotion, 3 oz. (85 g), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955092032, NDC 57955-0920-3
Manufacturer
King Bio Inc.
Category
Drug — Topical Medication
Hazard
Affected units
1,732

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: 013018ZZ Exp. 01/20
  • 021217ZZ Exp. 02/19
  • 110717ZZ Exp. 11/19

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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