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 .
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
View Memphis, TN recalls.
Back To Memphis