Data Foundry

Drug recalls 2019

Dr — Class I drug recall D-0521-2019

Terminated recall by King Bio Inc., reported 2019-03-20, distributed nationwide. Microbial contamination

Recall numberD-0521-2019
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmKing Bio Inc., Asheville, NC, United States
Recall initiated2018-07-20
Classified2019-03-08
Reported by FDA2019-03-20
Terminated2022-01-19
DistributedNationwide (US)
Countries outside the USAU, CA
Quantity105,716 bottles
Reason classesmicrobial contamination
NDC57955-8020-89
Lot numbers01/19, 01/20, 010716A, 011617H, 012517M, 02/19, 02/20, 020717A, 021816A, 03/19, 03/20, 030818B, 031016C, 031016D, 033016K, 05/19, 05/20, 052516J, 052918G, 06/19, 06/20, 062116A, 062818A, 062818E, 062818F, 090816B, 10/19, 101017G, 101216A, 102017C, 11/18, 11/19, 111417C, 112315A, 112916C, 12/19, 120217R, 120816N, 122817B

Product

Dr. King's aquaflora Candida High Potency, 8 fl. oz. (236 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806 USA, UPC 35795580018, NDC 57955-8020-89

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-0521-2019. 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.