MAX Brand LIVERAID
Recalling firm: Healthmaxx Global Inc.
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.
The exact product
MAX Brand LIVERAID, 200 Count Bottle. Product labeling reads in part:"MAX LIVERAID Dietary Supplement 200 Counts***6 65176 35168 6***Manufactured in FDA Approved Facility For:HealthMax Products Co. Altadena, CA 91001***".
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot # L0126 UPC 6 65176 35168 6
| Type | Code / value | Context |
|---|---|---|
| UPC | 665176351686 | Lot # L0126 UPC 6 65176 35168 6 |
| lot | L0126 | Lot # L0126 UPC 6 65176 35168 6 |
Recall details
- Recall number
- F-1922-2013
- Event ID
- 65733
- FDA status
- Terminated
- Initiated
- Jun 10, 2013
- Reported
- Oct 2, 2013
- Classified
- Sep 24, 2013
- Terminated
- Nov 14, 2014
- Quantity
- 3197 bottles
- Location
- Hacienda Heights, CA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
CA, MD, and NY
Data updated September 16, 2026. View official FDA data ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.