Dr. King's SafeCare Rx Liver Detox, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955006220, NDC 57955-0062-2

Recall Insight

This FDA Drug action (record #D-0864-2019) was formally reported on March 20, 2019, with the manufacturer initiating the action on July 20, 2018. It is classified under Critical severity (Class I), with a current status of Terminated. King Bio Inc. is listed as the recalling firm, operating out of Asheville, NC. Federal records indicate 875 bottles units are affected.

The documented reason for this recall is: Microbial contamination Distribution data in the federal record shows the product reached: U.S.A. Nationwide, Canada, and Australia.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC, NHTSA and USDA FSIS going back to 1995. Within the same product category, the database holds 6 closely related recalls. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 7 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.