Recalled by Healthmaxx Global Inc. · Hacienda Heights, CA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained; 2)ingredients listed are not actual ingredients contained.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgels; MAX Brand LIVER STRONG, 200 Count Softgels. Product labeling reads in part:"LIVERAID***Dietary Supplement 200 Softgels***6 65176 82031 1***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"LIVER AID***DIETARY SUPPLEMENT 200 Softgels***6 65176 02434***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"MAX LIVER STRONG***Dietary Supplment 200 Softgels***0 65176 06068 5***Manufactured in FDA Approved GMP Facility for:HealthMax Products Co. Altadena, CA 91001***".
Quantity: 5775 bottles
Food: Dietary supplements
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot # LS1227 UPCs: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068 5
California Maryland New York
FDA's distribution note: CA, MD, and NY
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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.
FDA files each product of one recall action separately; these share the same FDA event.
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
Reason In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: 1) product named on the label is not actual product contained…
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