King Bio Homeopathic Allergy Product Recalled for Microbial Contamination
King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Regional Allergies Desert U.S. due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class I, which indicates a reasonable probability that use of the product will cause serious adverse health consequences or death. Per the rubric, FDA Class I recalls are assigned a severity score of 4 or higher.
Plain-English summary
King Bio Inc. is recalling 5,984 bottles of Dr. King's Natural Medicine Homeopathic Regional Allergies Desert U.S., 2 fl. oz. (59 mL). The recall is being conducted because the product is subject to microbial contamination.
The affected product is identified by NDC 57955-8196-2 and UPC 357955518822. Specific lot numbers and expiration dates include 030916Q (Exp. 03/19), 052616A (Exp. 05/19), 072516J (Exp. 07/19), 072815B (Exp. 07/18), 012918A (Exp. 01/20), and 030817J (Exp. 03/19).
The product was distributed nationwide in the United States, as well as in Canada and Australia. Consumers should check their inventory for these specific lot numbers and expiration dates. If the product is found, consumers should stop using it and follow instructions from the recalling firm or the FDA regarding disposal or return.
The recalled product
- Product
- Dr. King's Natural Medicine Homeopathic Regional Allergies Desert U.S., 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955518822, NDC 57955-8196-2
- Manufacturer
- King Bio Inc.
- Category
- Drug — Homeopathic Medicine
- Hazard
- Affected units
- 5,984
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 (6)
- Lot Numbers: 030916Q Exp. 03/19
- 052616A Exp. 05/19
- 072516J Exp. 07/19
- 072815B Exp. 07/18
- 012918A Exp. 01/20
- 030817J Exp. 03/19
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 →- CriticalVictory Medical Center Pharmacy Recalls Glutathione Vials Due to Contamination
FDA (Drugs) · 2026-08-19
- HighMedline Medical Convenience Kits Recalled Due to Potential Bacillus Contamination
FDA (Devices) · 2026-07-29
- HighMedline Convenience Kits Recalled Over Bacillus Contamination
FDA (Devices) · 2026-07-29
- HighROHTO Cooling Eye Drops Recalled Over Sterility Assurance Concerns
FDA (Drugs) · 2026-07-29
- SeverePemetrexed for Injection Recalled Due to Lack of Sterility Assurance
FDA (Drugs) · 2026-07-15