RegeneArouse recall

Recalled by VivaCeuticals, Inc. dba Regeneca Worldwide · Irvine, CA, United States

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

Why it was recalled

The firm is recalling all herbal and dietary supplements because they were not manufactured in compliance with the current Good Manufacturing Practice regulations for Dietary Supplements.

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

RegeneArouse

Quantity: unknown

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.

all lots

Where it was sold

FDA's distribution note: US

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: VivaCeuticals, Inc. dba Regeneca Worldwide
Initiated by: Voluntary: Firm initiated
Recall initiated: Mar 9, 2017
In FDA report of: Apr 12, 2017
Terminated: Aug 8, 2017
FDA recall number: F-1821-2017 · event 76634
Official record: FDA enforcement report search

Also recalled with it (6 more products)

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

Class II · Moderate risk Terminated Processing Mar 9, 2017