King Bio Homeopathic Skin Irritations Recalled for Microbial Contamination
King Bio Inc. is recalling 2,177 bottles of Dr. King's Natural Medicine Homeopathic Skin Irritations & Itch Relief due to microbial contamination.
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.
Plain-English summary
King Bio Inc. is recalling 2,177 bottles of Dr. King's Natural Medicine Homeopathic Skin Irritations & Itch Relief, 2 fl. oz. (59 mL). The recall is due to microbial contamination.
The affected product is identified by NDC 57955-5168-2 and UPC 357955516828. Specific lot numbers and expiration dates are: 010818C (Exp. 01/20), 030916S (Exp. 08/18), 041117K (Exp. 04/19), 072216M (Exp. 07/19), and 083115F (Exp. 08/18).
The product was distributed nationwide in the U.S.A., as well as in Canada and Australia. Consumers should stop using the product and contact the manufacturer for instructions on return or disposal.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Skin Irritations & Itch Relief, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955516828, NDC 57955-5168-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic
- Hazard
- Affected units
- 2,177
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: 010818C Exp. 01/20
- 030916S Exp. 08/18
- 041117K Exp. 04/19
- 072216M Exp. 07/19
- 083115F Exp. 08/18
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
Same manufacturer · King Bio Inc.
See all →- CriticalKing Bio Recalls Dr. King's SafeCare Rx Calloused Due to Microbial Contamination
FDA (Drugs) · 2019-03-20
- SevereKing Bio Homeopathic Allergy Spray Recalled for Microbial Contamination
FDA (Drugs) · 2019-03-20
- CriticalKing Bio Recalls Heartburn Relief for Microbial Contamination
FDA (Drugs) · 2019-03-20
- SevereKing Bio Homeopathic Allergy Product Recalled for Microbial Contamination
FDA (Drugs) · 2019-03-20
- CriticalDr. King's Advanced Arnica Recalled for Microbial Contamination
FDA (Drugs) · 2019-03-20
Same hazard · microbial contamination
See all →- HighSV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination
FDA (Drugs) · 2026-10-07
- HighSV Labs Recalls Benzoyl Peroxide Wash Due to Microbial Contamination
FDA (Drugs) · 2026-10-07
- SevereMedline Ultrasound Breast Pack Recalled for Potential Sterility Breach
FDA (Devices) · 2026-09-09
- HighMedline Convenience Kits Recalled for Potential Sterility Breach
FDA (Devices) · 2026-09-09
- CriticalOptimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials
FDA (Drugs) · 2026-09-09
Similar recalls
- ModerateBeaumont Bio-Med Recalls Skin Irritation Homeopathic Spray Due to CGMP Deviations
FDA (Drugs) · 2018-09-26
- SevereFDA Recalls Energique Homeopathic Skin Spray Due to Microbial Contamination
FDA (Drugs) · 2016-01-27
- SevereKingston Pharma Recalls Infant Cough Syrup Due to Microbial Contamination
FDA (Food) · 2019-05-08
- SevereSprayology Recalls Body Skin Tonic Due to Potential Microbial Contamination
FDA (Drugs) · 2018-11-07
- SevereSuperior Pain & Itch Relief Lidocaine Gel Recalled for Contamination
FDA (Drugs) · 2019-09-25
- ModerateBioLyte Recalls NeoRelief Topical Gel Due to Ingredient Contamination
FDA (Drugs) · 2018-10-10