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…

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 Brand SOY ISOFLAVONES, 90 Count Capsules; MAX Brand ULTRA PROBIOTICS, 90 Count Capsules Product labeling reads in part:"MAX SOY ISOFLAVONES MENOPAUSE SUPPORT**DIETARY SUPPLEMENT 90 CAPSULES***6 65176 53126 2***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX ULTRA PROBIOTICS***90 Capsules Dietary Supplement***6 65176 30625 9***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".

FDA code information

Lot # P0912 UPCs: 6 65176 53126 2 and 6 65176 53126 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 Brand SOY ISOFLAVONES, 90 Count Capsules; MAX Brand ULTRA PROBIOTICS, 90 Count Capsules Product labeling reads in part:"MAX SOY ISOFLAVONES MENOPAUSE SUPPORT**DIETARY SUPPLEMENT 90 CAPSULES***6 65176 53126 2***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***". Product labeling reads in part:"MAX ULTRA PROBIOTICS***90 Capsules Dietary Supplement***6 65176 30625 9***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".

Extracted codes and context

TypeCode / valueContext
lotP0912Lot # P0912 UPCs: 6 65176 53126 2 and 6 65176 53126 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-1939-2013
Event ID
65733
FDA status
Terminated
Initiated
Jun 10, 2013
Reported
Oct 2, 2013
Classified
Sep 24, 2013
Terminated
Nov 14, 2014
Quantity
6,379 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-1939-2013

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

Follow official FDA and manufacturer guidance.