D-0718-2019 Class I Terminated
FDA drug recall D-0718-2019 was initiated by King Bio Inc. on July 20, 2018 and is designated Class I. Reason for recall: Microbial contamination The recall status is terminated (terminated January 19, 2022). Affected quantity: 92 bottles.
Recall Details
- Product Type
- Drugs
- Report Date
- March 20, 2019
- Initiation Date
- July 20, 2018
- Termination Date
- January 19, 2022
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 92 bottles
Product Description
Dr. King's SafeCare Rx M3 Metabolic Mineral Modulator, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955027621, NDC 57955-0277-2
Reason for Recall
Microbial contamination
Distribution Pattern
U.S.A. Nationwide, Canada, and Australia.
Code Information
Lots: 022216B Exp. 02/19; 062216S Exp. 06/19; 011217B Exp. 01/20