Class IIITerminated in FDA datasetRecall initiated Jun 10, 2013

Max Probiotic-90 tablets

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.

ProductMax Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products Inc. Altadena, CA 91001
UPC665176306259

FDA code information

Lot# PMG 0922

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Full FDA record and distribution details

Original product description

Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products Inc. Altadena, CA 91001

Extracted codes and context

TypeCode / valueContext
UPC665176306259Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT***Manufactured for:HealthMax Products Inc. Alt

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-1943-2013
Event ID
65733
FDA status
Terminated
Initiated
Jun 10, 2013
Reported
Oct 2, 2013
Classified
Sep 24, 2013
Terminated
Nov 14, 2014
Quantity
unknown
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-1943-2013

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

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