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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 65733

28 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 10, 2013
Product types
Food
Classifications
Class I, Class II, and Class III
Statuses
Terminated
Recalling firm wording
Healthmaxx Global Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

28 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 28

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***".

F-1916-2013
Recall number
F-1916-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
7,074 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # D0915

Distribution pattern

CA, MD, and NY

food · product 2 of 28

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***".

F-1917-2013
Recall number
F-1917-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
18,876 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # G0806 UPC 6 65176 08218 4

Distribution pattern

CA, MD, and NY

food · product 3 of 28

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***".

F-1918-2013
Recall number
F-1918-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
3,835 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # GL0214 UPC 6 65176 36159 3

Distribution pattern

CA, MD, and NY

food · product 4 of 28

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***"

F-1919-2013
Recall number
F-1919-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # G1212 UPC 6 65176 60566 6

Distribution pattern

CA, MD, and NY

food · product 5 of 28

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***".

F-1921-2013
Recall number
F-1921-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
5775 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # LS122 UPC: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068

Distribution pattern

CA, MD, and NY

food · product 6 of 28

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***".

F-1922-2013
Recall number
F-1922-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
3197 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # L0126 UPC 6 65176 35168 6

Distribution pattern

CA, MD, and NY

food · product 7 of 28

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***".

F-1923-2013
Recall number
F-1923-2013
Initiated
June 10, 2013
Classification
Class I
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
4139 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # S0703 UPC 0 65176 06756 1

Distribution pattern

CA, MD, and NY

food · product 8 of 28

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***".

F-1924-2013
Recall number
F-1924-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
2318 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # BP0417 UPC 6 65176 31465 0

Distribution pattern

CA, MD, and NY

food · product 9 of 28

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***".

F-1925-2013
Recall number
F-1925-2013
Initiated
June 10, 2013
Classification
Class II
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
9069 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # CL0925 UPC 0 65176 08108 6

Distribution pattern

CA, MD, and NY

food · product 10 of 28

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***".

F-1926-2013
Recall number
F-1926-2013
Initiated
June 10, 2013
Classification
Class II
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
2863 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # F0202 UPC 6 65176 05274 3

Distribution pattern

CA, MD, and NY

food · product 11 of 28

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***".

F-1927-2013
Recall number
F-1927-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
817 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # LIN0130 UPC 6 65176 01115 3

Distribution pattern

CA, MD, and NY

food · product 12 of 28

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***".

F-1928-2013
Recall number
F-1928-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
5775 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # LS1227 UPCs: 6 65176 82031 1, 6 65176 02434 4, and 0 65176 06068 5

Distribution pattern

CA, MD, and NY

food · product 13 of 28

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

F-1929-2013
Recall number
F-1929-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
31,259 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # SC0516 Exp. Date: Dec 2016 No UPC Code

Distribution pattern

CA, MD, and NY

food · product 14 of 28

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***".

F-1930-2013
Recall number
F-1930-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
6,126 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # H0411 UPC 6 65176 30162 9

Distribution pattern

CA, MD, and NY

food · product 15 of 28

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***".

F-1931-2013
Recall number
F-1931-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
2,245 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # T101612 UPC 0 65176 26512 7

Distribution pattern

CA, MD, and NY

food · product 16 of 28

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***".

F-1932-2013
Recall number
F-1932-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
4,531 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # ML1128 UPC 6 65176 32608 0

Distribution pattern

CA, MD, and NY

food · product 17 of 28

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***".

F-1933-2013
Recall number
F-1933-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
1,746 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

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

Distribution pattern

CA, MD, and NY

food · product 18 of 28

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***".

F-1934-2013
Recall number
F-1934-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
5,223 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # R1018 UPC 0 65176 55958 5

Distribution pattern

CA, MD, and NY

food · product 19 of 28

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***".

F-1935-2013
Recall number
F-1935-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
5,124 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # B0711 UPC 6 65176 62165 9

Distribution pattern

CA, MD, and NY

food · product 20 of 28

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***".

F-1936-2013
Recall number
F-1936-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
4,022 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # C1029 UPC 6 65176 33261 6

Distribution pattern

CA, MD, and NY

food · product 21 of 28

MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIETARY SUPPLEMENT 300 Capsules***0 65176 51257 3***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".

F-1937-2013
Recall number
F-1937-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
3,816 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # OP0921 UPC 0 65176 51257 3

Distribution pattern

CA, MD, and NY

food · product 22 of 28

MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***0 65176 30325 6".

F-1938-2013
Recall number
F-1938-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
2,659 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # A0830 UPC 0 65176 30325 6

Distribution pattern

CA, MD, and NY

food · product 23 of 28

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***".

F-1939-2013
Recall number
F-1939-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
6,379 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # P0912 UPCs: 6 65176 53126 2 and 6 65176 53126 2

Distribution pattern

CA, MD, and NY

food · product 24 of 28

MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:"MAX CoQ-10 80 mg***DIETARY SUPPLEMENT 300 Capsules***6 65176 25166 5***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***".

F-1940-2013
Recall number
F-1940-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
8,059 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # L0228 UPCs: 6 65176 25166 5

Distribution pattern

CA, MD, and NY

food · product 25 of 28

Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 150 tablets***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***".UPC 6 65176 52047 1

F-1941-2013
Recall number
F-1941-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
Unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot# D0915

Distribution pattern

CA, MD, and NY

food · product 26 of 28

Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:"*DIETARY SUPPLEMENT 100 capsules***Manufactured for:HealthMax Products Inc. Altadena, CA 91001***".UPC 0 65176 26289 8

F-1942-2013
Recall number
F-1942-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot# PMG 0922

Distribution pattern

CA, MD, and NY

food · product 27 of 28

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

F-1943-2013
Recall number
F-1943-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot# PMG 0922

Distribution pattern

CA, MD, and NY

food · product 28 of 28

MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:"MAX KIDNEY STRONG***Dietary Supplement 120 Tablets***6 65176 13427 2***Manufactured for: HealthMax Products, Inc. Altadena, CA 91001***".

F1920-2013
Recall number
F1920-2013
Initiated
June 10, 2013
Classification
Class III
Status
Terminated
Recalling firm
Healthmaxx Global Inc.
Quantity
1972 bottles

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mislabeling

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Lot # T2K002 UPC 6 65176 13427 2

Distribution pattern

CA, MD, and NY

Field note

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