King Bio Recalls Homeopathic Jet Lag Product Due to Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change 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 recall is classified as FDA Class I, which meets the rubric criteria for a Critical severity score (5).
Plain-English summary
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change, 2 fl. oz. (59 mL), due to microbial contamination. The recall involves 377 bottles of the product, identified by Lot 060216D with an expiration date of 06/19. The product is manufactured by King Bio Inc. and carries NDC 57955-5126-2 and UPC 357955512622.
The affected product was distributed nationwide in the United States, as well as in Canada and Australia. The U.S. Food and Drug Administration has classified this recall as Class I, indicating 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 check their lot numbers and expiration dates. If the product matches the recalled lot, consumers should stop using it and contact the manufacturer for further instructions or a refund.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Jet Lag & Shift Change, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955512622, NDC 57955-5126-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 377
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 (1)
- Lots: 060216D 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 →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
- CriticalFDA Recalls Compulsin Homeopathic OTC Medicine Due to Microbial Contamination
FDA (Drugs) · 2018-09-19
- ModerateKing Systems Recalls Adult Silicone King LAD Devices Due to Sterilization Indicator Issues
FDA (Devices) · 2012-11-28
- ModerateKing Systems Recalls Flexible ClearSeal Laryngeal Airway Devices
FDA (Devices) · 2012-11-28
- ModerateBioLyte Recalls NeoRelief Topical Gel Due to Ingredient Contamination
FDA (Drugs) · 2018-10-10
- CriticalFDA Recalls Respitrol Homeopathic Medicine Due to Microbial Contamination
FDA (Drugs) · 2018-09-19
- HighKing Systems Recalls Laryngeal Airway Devices Due to Sterilization Indicator Failure
FDA (Devices) · 2012-11-28