Recalls / Class I
Class IF-1923-2013
Class I— FDA's most serious classification, issued when there is a reasonable probability that consumption of or exposure to the product will cause serious adverse health consequences or death.
Product
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***".
- Type
- Food
- Affected lot / code info
- Lot # S0703 UPC 0 65176 06756 1
- Quantity
- 4139 bottles
Why it was recalled
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.
Recalling firm
- Firm
- Healthmaxx Global Inc.
- Notification channel
- Letter
- Type
- Voluntary: Firm initiated
- Address
- 16231 Elza Dr., N/A, Hacienda Heights, California 91745
Distribution
- Distribution pattern
- CA, MD, and NY
Timeline
- Recall initiated
- 2013-06-10
- FDA classified
- 2013-09-24
- Posted by FDA
- 2013-10-02
- Terminated
- 2014-11-14
- Status
- Terminated
Source: openFDA Food Enforcement endpoint. Recall record F-1923-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings.