FDAFDA · Food and drugs·Recall number F-1927-2013
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***".
Published October 2, 2013 · Recall initiated: June 10, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Healthmaxx Global Inc.
- Distributor
- CA, MD, and NY
- Lot
- Lot # LIN0130 UPC 6 65176 01115 3
- Risk classification
- Class III
- Area (FDA)
- food
- Country
- United States
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