Class IITerminated in FDA datasetJun 20, 2013

Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES

Recalling firm: Beta Labs

Why it was recalled

The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.

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ProductOxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599747
UPC670541599747

FDA code information

Lot #s 200910 and 200911, Exp 10/16

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Full FDA record and distribution details

Original product description

Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599747

Extracted codes and context

TypeCode / valueContext
UPC670541599747XTENDED RELEASE CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599747

Recall details

Recall number
F-2398-2014
Event ID
65585
FDA status
Terminated
Initiated
Jun 20, 2013
Reported
Sep 3, 2014
Classified
Aug 27, 2014
Terminated
Dec 3, 2014
Quantity
5951 units
Location
Memphis, TN, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

nationwide and UK

FDA source record · F-2398-2014

Data updated September 16, 2026. View official FDA data ↗

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