CLASS I Food recall · Reported 3 Sep 2014 · FDA Enforcement Report

Phentalene (TM), Pharmaceutical Grade, With 50 mg of Ephedra Extract recalled

Beta Labs is recalling Phentalene (TM), Pharmaceutical Grade, With 50 mg of Ephedra Extract, distributed nationwide in the US. The recall was initiated on 20 Jun 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # 58800512, Exp 05/16
Quantity recalled2154 units

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2399-2014
FDA event ID
65585
Recalling firm
Beta Labs, Memphis, TN
Classification
Class I
Status
Terminated
Recall initiated
20 Jun 2013
FDA classified
27 Aug 2014
Reported
3 Sep 2014
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Product category
Dietary Supplements

Timeline

20 Jun 2013Recall initiated by company
27 Aug 2014Classified by FDA+433 days
3 Sep 2014Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822

Where it was distributed

nationwide and UK

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

Lot # 58800512, Exp 05/16

Where was it sold?

nationwide and UK

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 65585

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