Healthmaxx Global — FDA Recall History & Enforcement Records
Data Notice: Recall frequency varies by category and firm size; data is comparative and may not indicate actual brand safety or quality. See Methodology.
As of July 16, 2026, Healthmaxx Global has 28 recorded FDA food enforcement actions in the openFDA database. Their most recent recall was on 10 Jun 2013. Healthmaxx Global is categorized under Supplements & Specialty based on their predominant recall history.
28
Total FDA recalls
13.1
Years in FDA database
2.1
Recalls per year
4,784 days(13.1 yrs)
Since last recall
3.6%
Class I (life-threatening)
2.1 recalls/yr vs Supplements & Specialty avg 2.3/yrBelow Average
Recall activity over time for Healthmaxx Global
How serious are Healthmaxx Global recalls?
FDA recall classifications by severity
Class I (Life-threatening)
3.6% (1 recalls)
Class II (Moderate risk)
7.1% (2 recalls)
Class III (Minor violation)
89.3% (25 recalls)
Full FDA recall history for Healthmaxx Global
All 28 FDA enforcement actions sourced from openFDA · Sorted by date, most recent first
| Date | Product | Reason | Class & Status |
|---|---|---|---|
| 10 Jun 2013Official FDA Notice | MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:”MAX RESVERATROL***Dietary Supplement 120 C | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Dietary Supplements under the same formulation, Labeled and Packaged in the Following: MAX Brand Proste-Support, 150 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Bio-Cell Collagen II, 100 Count Softgels Product labeling reads in part:”MAX Bio-Cell CollagenII Dietary Su | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:”MAX Nitric Oxide Enhance***DIETARY | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand GOUT AID, 130 Count Tablets Product labeling reads in part:”MAX GOUT AID***Dietary Supplement 130 Tablets** | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Hyper II DHA/EPA, 100 Count Softgels. Product labeling reads in part:”Hyper II DHA/EPA Refined Deep Sea Fish Oil 50% | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IITerminated |
| 10 Jun 2013Official FDA Notice | Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: LIVERAID, 200 Count Softgels; | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:”MAX LIVERAID Dietary Supplement 200 Counts***6 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand CoQ-10, 780mg, 300 Count Capsules. Product labeling reads in part:”MAX CoQ-10 80 mg***DIETARY SUPPLEMENT 30 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Glucosamine 1500 mg + MSM 400 mg, 120 Count Tablets. Product labeling reads in part:”MAX Triple Strength MO | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Max Probiotic-90 tablets UPC 6 65176 30625 9***Dietary Supplement Product labeling reads in part:”*DIETARY SUPPLEMENT*** | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Dietary Supplement labeled and packaged under the following: LIVERAID, 200 Count Softgels; LIVER AID, 200 Count Softgel | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Glucosamine 1500 mg, Plus MSM + Vit D 200 Count Tablets Product labeling reads in part:”MAX Glucosamine 150 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand CoQ10, 90 Count Capsules Product labeling reads in part:”MAX CoQ10***DIETARY SUPPLEMENT 90 Capsules***6 651 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Dietary Supplements Under the Same Formulation, Labeled and Packaged as the following: MAX LUNG AID, 100 Count Capsule | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Organic OPC69, 300 Count Capsules Product labeling reads in part:”MAX ORGANIC OPC69 MAXIMUM STRENGTH***DIET | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand BRAZILIAN BEE PROPOLIS, 180 Count Softgels Product labeling reads in part:”MAX***BRAZILIAN BEE PROPOLIS DIE | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Dietary Supplements Under the Same Formulation, Labeled and Packaged as the Following: MAX Brand SOY ISOFLAVONES, 90 Co | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand SUPER SELENIUM 250, 180 Count Tablets Product labeling reads in part:”MAX SUPER SELENIUM 250 ***Dietary Sup | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class ITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Organic Blueberry, 100 Count Capsules Product labeling reads in part:”MAX Organic Blueberry***Dietary Suppl | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX LIVER STRONG, 200 Count Capsules Product labeling reads in part:”MAX LIVER STRONG CoQ10***Dietary Supplement 200 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Kidney Strong, 120 Count Tablets Product labeling reads in part:”MAX KIDNEY STRONG***Dietary Supplement 120 | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Hyper II LECITHIN, 100 Count Softgels. Product labeling reads in part:”Hyper II LECITHIN***Dietary Supplement 100 Sof | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Max LUNG AID Extra Strength 100 capsules Dietary Supplement Product labeling reads in part:”*DIETARY SUPPLEMENT 100 caps | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Organic OPC31 Grapeseed Extract, 200 Count Capsules. Product labeling reads in part:”MAX Organic OPC31 Grap | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | Max Blood Sugar Defense 150 tablets Dietary Supplement Product labeling reads in part:”*DIETARY SUPPLEMENT 150 tablets** | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Glucosamine 1500 mg + MSM 400 mg, 300 Count Tablets. Product labeling reads in part:”MAX Triple Strength MO | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
| 10 Jun 2013Official FDA Notice | MAX Brand Stem Cell Enhance, 1.0 fl. oz. Product labeling reads in part:”MAX Stem Cell Enhance***1.0fl. oz(30ml)***”. | In response to a FDA inspection, the firm initiated this voluntary recall of various dietary supplements due to the following problems of mislabeling: | Class IIITerminated |
Where have Healthmaxx Global recalls occurred?
States affected across all recorded FDA enforcement actions
CA, MD, NY
Where does this recall data come from?
Verification required: FoodRecallFinder.com cannot verify the safety of individual food products in your possession. Always verify the current recall status at FDA.gov before disposing of or consuming a product.
Data sourced from the FDA Recall Enterprise System via openFDA API. This information is for educational purposes only and does not constitute health or legal advice. FoodRecallFinder.com is not affiliated with or endorsed by the U.S. Food and Drug Administration.
To determine if your specific product is affected, verify that the brand name, product description, lot number, UPC code, and date range all match the recall details exactly. When in doubt contact the recalling firm or visit FDA.gov.
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