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Healthmaxx Global Inc.

28 recall records on file.

2013

20 records

Class IIITerminatedRecall F-1916-2013

Product description

Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 Count Tablets. Product labeling reads in part:"Manufactured for: HealthMax Products Inc. 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.

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Event ID
65733
Code info
Lot # D0915
Product quantity
7,074 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1917-2013

Product description

MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg 120 Tablets***6 65176 08218 4***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.

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Event ID
65733
Code info
Lot # G0806 UPC 6 65176 08218 4
Product quantity
18,876 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1918-2013

Product description

MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:"MAX Triple Strength MOVE FREE Glucosamine 1500 mg + MSM 400 mg 300 Tablets***6 65176 36159 3***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.

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Event ID
65733
Code info
Lot # GL0214 UPC 6 65176 36159 3
Product quantity
3,835 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1919-2013

Product description

MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Glucosamine 1500mg***200 Tablets***6 65176 60566 6***Manufactured in FDA Approved facility for: HealthMax Products, Inc. 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.

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Event ID
65733
Code info
Lot # G1212 UPC 6 65176 60566 6
Product quantity
unknown
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1921-2013

Product description

Dietary Supplement labeled and packaged under 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 4***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***". Product labeling reads in part:"MAX LIVER STRONG Dietary Supplement 200 Softgels***0 65176 06068***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.

View full record
Event ID
65733
Code info
Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068
Product quantity
5775 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1922-2013

Product description

MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***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.

View full record
Event ID
65733
Code info
Lot # L0126 UPC 6 65176 35168 6
Product quantity
3197 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class ITerminatedRecall F-1923-2013

Product description

MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:"MAX SUPER SELENIUM 250 ***Dietary Supplement 180 Tablet***0 65176 06756 1***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.

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Event ID
65733
Code info
Lot # S0703 UPC 0 65176 06756 1
Product quantity
4139 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1924-2013

Product description

MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX***BRAZILIAN BEE PROPOLIS DIETARY SUPPLEMENT 180 Softgels***6 65176 31465 0***Manufactured 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.

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Event ID
65733
Code info
Lot # BP0417 UPC 6 65176 31465 0
Product quantity
2318 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IITerminatedRecall F-1925-2013

Product description

MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:"MAX Bio-Cell CollagenII Dietary Supplement 100 Softgels*** 0 65176 08108 6***Manufactured 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.

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Event ID
65733
Code info
Lot # CL0925 UPC 0 65176 08108 6
Product quantity
9069 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IITerminatedRecall F-1926-2013

Product description

Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hyper II DHA/EPA Refined Deep Sea Fish Oil 50% DHA - 30% EPA***Dietary Supplement 100 Softgels***6 65176 05274 3***Manufactured 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.

View full record
Event ID
65733
Code info
Lot # F0202 UPC 6 65176 05274 3
Product quantity
2863 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1927-2013

Product description

Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN***Dietary Supplement 100 Softgels***6 65176 01115 3***Manufactured 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.

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Event ID
65733
Code info
Lot # LIN0130 UPC 6 65176 01115 3
Product quantity
817 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1928-2013

Product description

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***".

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.

View full record
Event ID
65733
Code info
Lot # LS1227 UPCs: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068 5
Product quantity
5775 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1929-2013

Product description

MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance***1.0fl. oz(30ml)***".

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.

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Event ID
65733
Code info
Lot # SC0516 Exp. Date: Dec 2016 No UPC Code
Product quantity
31,259 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1930-2013

Product description

MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10***DIETARY SUPPLEMENT 90 Capsules***6 65176 30162 9***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.

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Event ID
65733
Code info
Lot # H0411 UPC 6 65176 30162 9
Product quantity
6,126 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1931-2013

Product description

MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID***Dietary Supplement 130 Tablets***6 0 65176 26512 7***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.

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Event ID
65733
Code info
Lot # T101612 UPC 0 65176 26512 7
Product quantity
2,245 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1932-2013

Product description

MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10***Dietary Supplement 200 Capsules***6 65176 32608 0***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.

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Event ID
65733
Code info
Lot # ML1128 UPC 6 65176 32608 0
Product quantity
4,531 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall 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.

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Event ID
65733
Code info
Lot # PMG022 UPC 0 65176 26289 8 and 0 65176 30266 2
Product quantity
1,746 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1934-2013

Product description

MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958 5***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.

View full record
Event ID
65733
Code info
Lot # R1018 UPC 0 65176 55958 5
Product quantity
5,223 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1935-2013

Product description

MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:"MAX Organic Blueberry***Dietary Supplement 100 CAPSULES***6 65176 62165 9***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.

View full record
Event ID
65733
Code info
Lot # B0711 UPC 6 65176 62165 9
Product quantity
5,124 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014
Class IIITerminatedRecall F-1936-2013

Product description

MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:"MAX Organic OPC31 Grapeseed Extract***NEW WITH BLUEBERRY***Dietary Supplement 200 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. 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.

View full record
Event ID
65733
Code info
Lot # C1029 UPC 6 65176 33261 6
Product quantity
4,022 bottles
Distribution pattern
CA, MD, and NY
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
16231 Elza Dr., N/A, Hacienda Heights, CA, United States
Recall initiation date
06/10/2013
Center classification date
09/24/2013
Termination date
11/14/2014