Q-min, 50 capsules per plastic bottle recall

Recalled by Basic Reset Inc. · Hendersonville, TN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Products do not conform to Dietary Supplement CGMP regulations.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Q-min, 50 capsules per plastic bottle, SKU: 100-9B

Quantity: N/A

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

170801-BSC0462

Where it was sold

Nationwide.

Puerto Rico

FDA's distribution note: 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.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: Basic Reset Inc.
Initiated by: FDA Mandated
Recall initiated: Sep 23, 2019
In FDA report of: Nov 27, 2019
Terminated: Aug 19, 2020
FDA recall number: F-0182-2020 · event 83917
Official record: FDA enforcement report search

Also recalled with it (13 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class II · Moderate risk Terminated Processing Sep 23, 2019