Aquaflora Phase II Candida Control Program — Class I drug recall D-0901-2019
Terminated recall by King Bio Inc., reported 2019-03-20, distributed nationwide. Microbial contamination
| Recall number | D-0901-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | King Bio Inc., Asheville, NC, United States |
| Recall initiated | 2018-07-20 |
| Classified | 2019-03-08 |
| Reported by FDA | 2019-03-20 |
| Terminated | 2022-01-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 2,248 bottles |
| Reason classes | microbial contamination |
| UPC / GTIN / UDI-DI | 00357955160267 |
| NDC | 57955-1602-06 |
| Lot numbers | 01/20, 010518G, 011617F, 02/19, 021016G, 051716P, 07/18, 072315A |
Product
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 57955-1602-6
Reason for recall
Microbial contamination
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0901-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.