Drug recall
Aquaflora Heavy Metal Detox Candida, 2 fl. oz. (59 mL), Homeopathic, King Bio, Inc. 3 Westside Dr. Asheville…
FDA recall event 80601 · Class I · King Bio Inc.
Key facts
| Event ID | 80601 |
|---|---|
| Recall numbers | D-0521-2019, D-0522-2019, D-0523-2019, D-0524-2019, D-0525-2019, D-0526-2019, D-0527-2019, D-0528-2019, D-0529-2019, D-0530-2019, D-0531-2019, D-0532-2019 and 453 more |
| Recalling firm | King Bio Inc. |
| Product type | Drugs |
| Products | Aquaflora Heavy Metal Detox Candida, 2 fl. oz. (59 mL), Homeopathic, King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, NDC 57955-2281-2, Aquaflora High Potency Candida Control Program Homeopathic Formula, Net 16 fl. oz. (1 pt) 473 mL, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955160366, NDC…, Aquaflora Phase I Candida Control Program, Net 16 fl. oz. (1 PT) 473 mL, Homeopathic Formula, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955160168, NDC 57955-1601-6, Aquaflora Phase II Candida Control Program, Net 16 fl. oz. (1 PT) 473 mL, Homeopathic Formula, Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955160267, NDC…, Dr. King's Acute Pain Relief Cooling Topical, 89 mL (topical cream), Manufactured by: King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 Imported by Ambiental Solutions, Inc. Vancouver, BC, V5Y 1E6… and 457 more |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Microbial contamination |
| Initiation date | Jul 20, 2018 |
| Report date | Mar 20, 2019 |
| Termination date | Jan 19, 2022 |
| City | Asheville |
| State | NC |
| Country | United States |
| FEI number | 1053442 |
At a glance
- 100–999 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: