PlainRecalls
FDA Food Low Class III Terminated

Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count Capsules. Product labeling reads in part:"MAX LUNG AID Extra Strength Dietary Supplement 100 CAPSULES***0 65176 26289 8***HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX POMEGRANATE DIETARY SUPPLEMENT 100 CAPSULES***0 65176 30266 2***Manufactured in FDA Approved Facility For:HealthMax Products Co. Alt

Reported: October 2, 2013 Initiated: June 10, 2013 #F-1933-2013

Product Description

Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count Capsules. Product labeling reads in part:"MAX LUNG AID Extra Strength Dietary Supplement 100 CAPSULES***0 65176 26289 8***HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX POMEGRANATE DIETARY SUPPLEMENT 100 CAPSULES***0 65176 30266 2***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".

Reason for Recall

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.

Details

Recalling Firm
Healthmaxx Global Inc.
Units Affected
1,746 bottles
Distribution
CA, MD, and NY
Location
Hacienda Heights, CA

Frequently Asked Questions

What product was recalled? ▼
Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsules; MAX Brand POMEGRANATE, 100 Count Capsules. Product labeling reads in part:"MAX LUNG AID Extra Strength Dietary Supplement 100 CAPSULES***0 65176 26289 8***HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX POMEGRANATE DIETARY SUPPLEMENT 100 CAPSULES***0 65176 30266 2***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".. Recalled by Healthmaxx Global Inc.. Units affected: 1,746 bottles.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on October 2, 2013. Severity: Low. Recall number: F-1933-2013.

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