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Healthmaxx Global Inc.

Complete recall history across all FDA and CPSC categories — 28 total recalls

Healthmaxx Global Inc. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Food Recalls (28)

FDA food safety enforcement actions by Healthmaxx Global Inc.

Date Product Reason Class
Jun 10, 2013 MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:"M... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product lab... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product lab... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:"Hyp... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:"MAX L... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class I
Jun 10, 2013 Dietary Supplements Under the Same Formulation, Labeled and Packaged as the F... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling read... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Dietary Supplements Under the Same Formulation, Labeled and Packaged as the f... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:"MAX CoQ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Dietary Supplement labeled and packaged under the following: LIVERAID, 200 C... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product lab... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product lab... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in par... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Dietary Supplements Under the Same Formulation, Labeled and Packaged as the F... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:"Hype... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class II
Jun 10, 2013 MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:"MAX ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads i... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads ... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class II
Jun 10, 2013 Dietary Supplements under the same formulation, Labeled and Packaged in the F... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III
Jun 10, 2013 MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:... In response to a FDA inspection, the firm initiated this voluntary recall of ... Class III

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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