FDA Food recall F-2399-2014
PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670…
- FDA Food
- Class I
- terminated
- Published 2014-09-03
On 2014-09-03 the FDA classified a Class I recall of PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670… by Beta Labs, citing the products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-2399-2014 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-06-20 |
| Published | 2014-09-03 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | Beta Labs |
| Distribution | US |
Product
PHENTALENE (TM), PHARMACEUTICAL GRADE, With 50 mg of Ephedra Extract, 90 CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599822
Reason
The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Identifiers
| upc | 670541599822 |
|---|---|
| code_info | Lot # 58800512, Exp 05/16 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2399-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.