MAX Brand Nitric Oxide Enhance
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.
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065176559585FDA code information
Lot # R1018 UPC 0 65176 55958 5
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Full FDA record and distribution details
Original product description
MAX Brand Nitric Oxide Enhance, 90 Count Capsules Product labeling reads in part:"MAX Nitric Oxide Enhance***DIETARY SUPPLEMENT 90 Capsules***0 65176 55958 5***Manufactured in FDA Approved Facility for:HealthMax Products Co. Altadena, CA 91001***".
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 065176559585 | Lot # R1018 UPC 0 65176 55958 5 |
| lot | R1018 | Lot # R1018 UPC 0 65176 55958 5 |
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-1934-2013
- Event ID
- 65733
- FDA status
- Terminated
- Initiated
- Jun 10, 2013
- Reported
- Oct 2, 2013
- Classified
- Sep 24, 2013
- Terminated
- Nov 14, 2014
- Quantity
- 5,223 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 ↗
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