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Q-min, 50 capsules per plastic bottle, SKU: 100-9B: FDA Recall F-0182-2020

Agency action: Sep 23, 2019Record ID: F-0182-2020
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What happened

Original notice title

Q-min, 50 capsules per plastic bottle, SKU: 100-9B, recall F-0182-2020

From the archived source record

Products do not conform to Dietary Supplement CGMP regulations.

What the official notice says to do

Check the original notice for the instructions that apply to the named product, company, and affected lots.

Read the official notice →

Status and source details

Status recorded in the archive
Terminated
FDA recall classification
Class II
Recall initiated by
FDA Mandated
Report date
Nov 27, 2019
Termination date in the archive
Aug 19, 2020
Source checked
Jul 16, 2026
Record revision
4e05eb4a5fb4

This is a dated record. Its current status may have changed since the source was captured. A record applies to its stated scope; it is not a safety rating for every product from a company.

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Source presentation by Dr. Edward M.Kim, PharmD · Clinical Director, SupplementSafety editorial team · How we prepare records

What is affected

Product
Q-min, 50 capsules per plastic bottle, SKU: 100-9B
Company
Basic Reset Inc.
Lot / identifier
170801-BSC0462
Market / distribution
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.