Dino Min, 60 capsules per plastic bottle, SKU: 100-1C

Recall Insight

This FDA Food action (record #F-1239-2020) was formally reported on November 27, 2019, with the manufacturer initiating the action on September 23, 2019. It is classified under Moderate severity (Class II), with a current status of Terminated. Basic Reset Inc. is listed as the recalling firm, operating out of Hendersonville, TN. Federal records indicate N/A units are affected.

The documented reason for this recall is: Products do not conform to Dietary Supplement CGMP regulations. Distribution data in the federal record shows the product reached: Product was shipped to all 50 states. Product was shipped to the following foreign consignees: Canada, Nigeria, U.K., Australia, Israel, Puerto Rico, Virgin Islands, Hungary, UAE, Mexico, Philippines, Greece, and Puerto…. 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.