FDA recall record

Basic Reset Dino Min, 60 capsules per plastic bottle, SKU: 100-1C recall — FDA F-1239-2020

Products do not conform to Dietary Supplement CGMP regulations.

Class IIclassification
F-1239-2020official record ID
Nov 27, 2019report date

Recall record at a glance

Official recordF-1239-2020
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBasic Reset Inc.
Report dateNov 27, 2019
Recall initiation dateSep 23, 2019
QuantityN/A
LocationHendersonville, TN, United States

Official product description

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

Why the product was recalled

Products do not conform to Dietary Supplement CGMP regulations.

Distribution information

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.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: FDA Mandated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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