Check the Batch
Class IIITerminated in FDA datasetRecall initiated Jun 10, 2013

Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG…

Recalling firm: Healthmaxx Global Inc.

Why it was 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…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 14, 2014.

Check your package

Compare the exact product and package details with the label you have.

ProductDietary 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***".
UPC065176262898

FDA code information

Lot # PMG022 UPC 0 65176 26289 8 and 0 65176 30266 2

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original 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***".

Extracted codes and context

TypeCode / valueContext
UPC065176262898Lot # PMG022 UPC 0 65176 26289 8 and 0 65176 30266 2
lotPMG022Lot # PMG022 UPC 0 65176 26289 8 and 0 65176 30266 2

Original FDA recall 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; 2)ingredients listed are not actual ingredients contained.

Recall details

Recall number
F-1933-2013
Event ID
65733
FDA status
Terminated
Initiated
Jun 10, 2013
Reported
Oct 2, 2013
Classified
Sep 24, 2013
Terminated
Nov 14, 2014
Quantity
1,746 bottles
Location
Hacienda Heights, CA, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

CA, MD, and NY

FDA source record · F-1933-2013

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.