PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822
Reported: September 3, 2014 Initiated: June 20, 2013 #F-2399-2014
Product Description
PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822
Reason for Recall
The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Details
- Recalling Firm
- Beta Labs
- Units Affected
- 2154 units
- Distribution
- nationwide and UK
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822. Recalled by Beta Labs. Units affected: 2154 units.
Why was this product recalled? ▼
The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on September 3, 2014. Severity: Critical. Recall number: F-2399-2014.
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