How many FDA recalls has Healthmaxx Global Inc. had?

The FDA has published 28 food recall enforcement records naming Healthmaxx Global Inc. between 2013 and 2013. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.

Does a high recall count mean a firm is unsafe?

Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

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Healthmaxx Global Inc. FDA recall records

The FDA has published 28 food recall enforcement records naming Healthmaxx Global Inc. between 2013 and 2013, covering 1 separate recall events. The firm is recorded in California. Data last updated 2 September 2026.

Records of 29,386: 28
Share of all recalls: 0.1%
Class I of 28: 1
Reported between: 2013 to 2013

What is different about Healthmaxx Global Inc.

The hazard that separates Healthmaxx Global Inc. from the national picture is undeclared allergens: 100% of these records name it, against 26.5% of all FDA food recalls.

By product, Healthmaxx Global Inc. is weighted toward dietary supplements: 85.7% of the records here against 6.2% across the corpus.

Recalls at Healthmaxx Global Inc. skew less severe than the corpus: 3.6% are Class I against 44% nationally.

A recall at Healthmaxx Global Inc. stays open a median of 522 days between the report and termination, against 215 days for the corpus as a whole. Termination follows the firm accounting for every unit of the affected lot.

These recalls stay local: 0% state nationwide distribution, against 20.7% across the corpus.

A single recall here covers far more records than usual: 28 enforcement records per FDA event, against 3.7 across the corpus. The agency opens one record per product code, so this is a sign of broad product lines rather than of repeated failures.

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 28 records cover 1 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

1 of these records are Class I, 2 Class II and 25 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

What was recalled for

A single record can name more than one hazard, so these counts overlap.

Undeclared allergens28

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Year	Recalls reported
2012	0
2013	28
2014	0
2015	0
2016	0
2017	0
2018	0
2019	0
2020	0
2021	0
2022	0
2023	0
2024	0
2025	0
2026	0

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

California28

Most recently reported

All 28 records.
Reported	Product	Firm	Reason	Class
2013-10-02	MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL*Dietary Supplement 120 CAPSULESManufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001**0 65176 30325 6".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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***".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 6Manufactured for:HealthMax Products Co. Altadena, CA 91001**".	Healthmaxx Global Inc.	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.	Class II
2013-10-02	MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance*DIETARY SUPPLEMENT 90 Capsules0 65176 55958 5Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX GOUT AID*Dietary Supplement 130 Tablets6 0 65176 26512 7HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 Softgels6 65176 05274 3Manufactured for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class II
2013-10-02	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 Softgels6 65176 82031 1Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001". Product labeling reads in part:"LIVER AIDDIETARY SUPPLEMENT 200 Softgels6 65176 02434Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001". Product labeling reads in part:"MAX LIVER STRONGDietary Supplment 200 Softgels0 65176 06068 5Manufactured in FDA Approved GMP Facility for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts*6 65176 35168 6Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001**".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:"MAX CoQ-10 80 mg*DIETARY SUPPLEMENT 300 Capsules6 65176 25166 5Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 4Manufactured in FDA Approved Facility for: HealthMax Products Co. Altadena, CA 91001**".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 Softgels6 65176 82031 1Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001". Product labeling reads in part:"LIVER AIDDIETARY SUPPLEMENT 200 Softgels6 65176 02434 4Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001". Product labeling reads in part:"MAX LIVER STRONG Dietary Supplement 200 Softgels0 65176 06068Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001**".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:"MAX Glucosamine 1500mg*200 Tablets6 65176 60566 6Manufactured in FDA Approved facility for: HealthMax Products, Inc. Altadena, CA 91001*"	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ10*DIETARY SUPPLEMENT 90 Capsules6 65176 30162 9Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 8HealthMax Products Inc. Altadena, CA 91001". Product labeling reads in part:"MAX POMEGRANATE DIETARY SUPPLEMENT 100 CAPSULES0 65176 30266 2Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:"MAX ORGANIC OPC69 MAXIMUM STRENGTH*DIETARY SUPPLEMENT 300 Capsules0 65176 51257 3Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:"MAX*BRAZILIAN BEE PROPOLIS DIETARY SUPPLEMENT 180 Softgels6 65176 31465 0Manufactured For:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 SUPPORTDIETARY SUPPLEMENT 90 CAPSULES6 65176 53126 2Manufactured for:HealthMax Products Inc. Altadena, CA 91001". Product labeling reads in part:"MAX ULTRA PROBIOTICS90 Capsules Dietary Supplement6 65176 30625 9Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:"MAX SUPER SELENIUM 250 *Dietary Supplement 180 Tablet0 65176 06756 1Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class I
2013-10-02	MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:"MAX Organic Blueberry*Dietary Supplement 100 CAPSULES6 65176 62165 9Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX LIVER STRONG CoQ10*Dietary Supplement 200 Capsules6 65176 32608 0Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:"MAX KIDNEY STRONG*Dietary Supplement 120 Tablets6 65176 13427 2Manufactured for: HealthMax Products, Inc. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyper II LECITHIN*Dietary Supplement 100 Softgels6 65176 01115 3Manufactured for:HealthMax Products Co. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:"DIETARY SUPPLEMENT 100 capsulesManufactured for:HealthMax Products Inc. Altadena, CA 91001*".UPC 0 65176 26289 8	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:"MAX Organic OPC31 Grapeseed Extract*NEW WITH BLUEBERRYDietary Supplement 200 CAPSULESManufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001*".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:"DIETARY SUPPLEMENT 150 tabletsManufactured for:HealthMax Products Inc. Altadena, CA 91001*".UPC 6 65176 52047 1	Healthmaxx Global Inc.	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.	Class III
2013-10-02	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 3Manufactured in FDA Approved Facility for: HealthMax Products Co. Altadena, CA 91001**".	Healthmaxx Global Inc.	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.	Class III
2013-10-02	MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"MAX Stem Cell Enhance*1.0fl. oz(30ml)*".	Healthmaxx Global Inc.	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.	Class III

Questions

How many FDA recalls has Healthmaxx Global Inc. had?: The FDA has published 28 food recall enforcement records naming Healthmaxx Global Inc. between 2013 and 2013. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?: Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.