FDA Drug recall D-165-2013
SLIMDIA Revolution capsules, 30-count capsules per bottle, Yerba Naturals, 19685 Varda Ave., Buena Park, CA
- FDA Drug
- Class I
- terminated
- Published 2013-02-27
On 2013-02-27 the FDA classified a Class I recall of SLIMDIA Revolution capsules, 30-count capsules per bottle, Yerba Naturals, 19685 Varda Ave., Buena Park, CA by P And J Trading, citing marketed Without an Approved NDA/ANDA: All lots of the dietary supplement Slimdia Revolution are being recalled because they contain sibutramine, a previously approved FDA drug re….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-165-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-12-19 |
| Published | 2013-02-27 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | P And J Trading |
| Distribution | n/a |
Product
SLIMDIA Revolution capsules, 30-count capsules per bottle, Yerba Naturals, 19685 Varda Ave., Buena Park, CA.
Reason
Marketed Without an Approved NDA/ANDA: All lots of the dietary supplement Slimdia Revolution are being recalled because they contain sibutramine, a previously approved FDA drug removed from the U.S. marketplace for safety reasons, making it an unapproved new drug.
Identifiers
| code_info | There are no manufacturing codes associated with the product. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-165-2013%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.