FDA Recalls King Bio Leg Cramp Relief Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Leg Cramp & Spasm Relief Homeopathic 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 5/5 (Critical).
Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.
Our severity reasoning: The FDA has classified this recall as Class I, which per the rubric mandates a severity score of 5 (Critical) regardless of other factors.
Plain-English summary
King Bio Inc. is recalling Dr. King's Natural Medicine Leg Cramp & Spasm Relief Homeopathic, 2 fl oz (59 mL), due to microbial contamination. The recall involves 9,405 bags of the product. Specific lots affected include 102816D (Exp. 10/19), 050516F (Exp. 05/19), 101416A (Exp. 10/19), 123115D (Exp. 12/18), and 041518J (Exp. 04/20).
The product was distributed nationwide in the United States, as well as in Canada and Australia. The FDA has classified this recall as Class I, which indicates a reasonable probability that use of or exposure to the violative product will cause serious adverse health consequences or death.
Consumers who have purchased this product should stop using it and contact King Bio Inc. for further instructions or a refund. The product is identified by UPC 357955543527 and NDC 57955-6035-2.
The recalled product
- Product
- Dr. King's Natural Medicine Leg Cramp & Spasm Relief Homeopathic, 2 fl oz (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955543527, NDC 57955-6035-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 9,405
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)
- Lots: 102816D Exp. 10/19
- 050516F Exp. 05/19
- 101416A Exp. 10/19
- 123115D Exp. 12/18
- 041518J Exp. 04/20
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
- ModerateHealthful Naturals Leg Cramp Support Oral Spray Recalled for CGMP Deviations
FDA (Drugs) · 2018-11-14
- ModerateBeaumont Bio-Med Recalls Muscle & Joint Pain Relief Spray for CGMP Deviations
FDA (Drugs) · 2018-09-26
- ModerateBioLyte Recalls NeoRelief Topical Gel Due to Ingredient Contamination
FDA (Drugs) · 2018-10-10
- ModerateBeaumont Bio-Med Recalls Arthritis Pain Relief Spray Due to CGMP Deviations
FDA (Drugs) · 2018-09-26
- SevereFDA Recalls Energique Homeopathic Pain Spray for Microbial Contamination
FDA (Drugs) · 2016-01-27
- SevereKingston Pharma Recalls Infant Cough Syrup Due to Microbial Contamination
FDA (Food) · 2019-05-08