D-0903-2019 Class I Terminated
FDA drug recall D-0903-2019 was initiated by King Bio Inc. on Jul 20, 2018 and is designated Class I. Reason for recall: Microbial contamination The recall status is terminated (terminated Jan 19, 2022). Affected quantity: 2634 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- Mar 20, 2019
- Initiation Date
- Jul 20, 2018
- Termination Date
- Jan 19, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2634 bottles
Product Description
Dr. King's Aquaflora Enzyme Restoration Upper GI Homeopathic, 2 fl. oz. (59 mL), King Bio, Inc. 3 Westside Dr. Asheville, NC 28806 USA, UPC 357955232124, NDC 57955-3321-2
Reason for Recall
Microbial contamination
Distribution Pattern
U.S.A. Nationwide, Canada, and Australia.
Code Information
Lots: 102016H Exp. 10/19; 010518E Exp. 01/20; 050616A Exp. 05/19
Source
- Dataset
- openFDA drug recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for D-0903-2019
- openFDA file date
- Oct 6, 2026
- Loaded by RegDataLab
- Oct 12, 2026