MAX Brand RESVERATROL
Recalling firm: Healthmaxx Global Inc.
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 14, 2014.
Check your package
Compare the exact product and package details with the label you have.
065176303256FDA code information
Lot # A0830 UPC 0 65176 30325 6
Match the product, package size, and code together. A missing match does not guarantee safety.
Full FDA record and distribution details
Original product description
MAX Brand RESVERATROL, 120 Count Capsules. Product labeling reads in part:"MAX RESVERATROL***Dietary Supplement 120 CAPSULES***Manufactured in FDA Approved Facility for:HealthMax Products Inc. Altadena, CA 91001***0 65176 30325 6".
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 065176303256 | Lot # A0830 UPC 0 65176 30325 6 |
| lot | A0830 | Lot # A0830 UPC 0 65176 30325 6 |
Original FDA recall reason
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.
Recall details
- Recall number
- F-1938-2013
- Event ID
- 65733
- FDA status
- Terminated
- Initiated
- Jun 10, 2013
- Reported
- Oct 2, 2013
- Classified
- Sep 24, 2013
- Terminated
- Nov 14, 2014
- Quantity
- 2,659 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 ↗
Follow official FDA and manufacturer guidance.