FDA recalls · F-2400-2014
Beta Labs recall
- FoodPHEnFX (TM), PHENO 550 mg, PHARMACEUTICAL GRADE, 90 CAPSULES, Manufactured for: Beta Labs, LTD, Newark, DE 19711, UPC 029882559802
- ReasonThe products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2014-12-03
- DatesFirm started it 2013-06-20. In FDA's enforcement report 2014-09-03.
- Sold innationwide and UK
- Amount743 units
- CodesLot # 1205129, Exp 12/16
- FirmBeta Labs, Memphis, TN · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-2400-2014. Class meanings: FDA.