Class IITerminated in FDA datasetRecall initiated Sep 23, 2019

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

Recalling firm: Basic Reset Inc.

Why it was recalled

Products do not conform to Dietary Supplement CGMP regulations.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 19, 2020.

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

FDA code information

02219A, 27418A, 22618B, 18919A, 11618B, 07819A, 06118D, 36017B

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Full FDA record and distribution details

Original product description

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

Original FDA recall reason

Products do not conform to Dietary Supplement CGMP regulations.

Recall details

Recall number
F-1239-2020
Event ID
83917
FDA status
Terminated
Initiated
Sep 23, 2019
Reported
Nov 27, 2019
Classified
Nov 21, 2019
Terminated
Aug 19, 2020
Quantity
N/A
Location
Hendersonville, TN, United States
Initiation type
FDA Mandated
Notification
E-Mail

Where it was distributed

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 Rico.

FDA source record · F-1239-2020

Data updated September 16, 2026. View official FDA data ↗

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