FDA Drug recall D-265-2013
Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
- FDA Drug
- Class I
- terminated
- Published 2013-04-24
On 2013-04-24 the FDA classified a Class I recall of Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA by Body Basics, citing marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-265-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2011-12-19 |
| Published | 2013-04-24 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Body Basics |
| Distribution | US |
Product
Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
Reason
Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction
Identifiers
| upc | 830733002016 |
|---|---|
| code_info | Lot number 008A, expiration date Dec 2014, UPC code 830733002016 |
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-265-2013%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.