Actra-SX 500 Capsules — Class I drug recall D-265-2013
Terminated recall by Body Basics Inc, reported 2013-04-24, distributed nationwide. Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved pro
| Recall number | D-265-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Body Basics Inc, Canoga Park, CA, United States |
| Recall initiated | 2011-12-19 |
| Classified | 2013-04-18 |
| Reported by FDA | 2013-04-24 |
| Terminated | 2013-06-05 |
| Distributed | Nationwide (US) |
| Quantity | 30,000 capsules |
| Reason classes | unapproved product |
| Lot numbers | 008A |
| Expiration dates | 2014-12-20 |
Product
Actra-SX 500 Capsules, Maximum Strength, Energizer, 500 mg, 5 count package, Body Basics, Canoga Park, CA
Reason for recall
Marketed without an Approved NDA/ANDA; product contains sildenafil, an active ingredient in a FDA approved product for the treatment of Erectile Dysfunction
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-265-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.