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Recall Number: F-2400-2014

Why was PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802 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-2400-2014 .

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 II

  • 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: PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802

  • Report Date: 2014-09-03

  • Product Type: Food

  • Company: Beta Labs

  • Status: Terminated

  • Recall Number: F-2400-2014

  • 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 # 1205129, Exp 12/16

  • Product Quantity: 743 units

  • Address: 2 W GE Patterson Ave Apt 103

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