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Recall Number: F-2399-2014

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

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

Check out this page for guidance on what to do if you've consumed food from recall F-2399-2014 .

Beta Labs recall in Memphis, TN details
Here's recall specific data. Click on the company, city, or state for more recalls by Beta Labs or more recalls in Memphis or Tennessee.

  • City: Memphis

  • State: Tennessee

  • Country: United States

  • Classification: Class I

  • Classification Date: 2014-08-27

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

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

  • Report Date: 2014-09-03

  • Product Type: Food

  • Company: Beta Labs

  • Status: Terminated

  • Recall Number: F-2399-2014

  • Postal Code: 38103-6429

  • Recall Initiation Date: 2013-06-20

  • Recall End Date: 2014-12-03

  • Event ID: 65585

  • Distribution Pattern: nationwide and UK

  • Voluntary Or Mandated: Voluntary: Firm initiated

  • Initial Firm Notification: Press Release

  • Extra Info: Lot # 58800512, Exp 05/16

  • Product Quantity: 2154 units

  • Address: 2 W GE Patterson Ave Apt 103

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