PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
Reported: September 3, 2014 Initiated: June 20, 2013 #F-2400-2014
Product Description
PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
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
- 743 units
- Distribution
- nationwide and UK
- Location
- Memphis, TN
Frequently Asked Questions
What product was recalled? ▼
PHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802. Recalled by Beta Labs. Units affected: 743 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: Moderate. Recall number: F-2400-2014.
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