BLUE Diamond Pill — Class I drug recall D-334-2013
Terminated recall by Performance Plus Marketing, Inc., reported 2013-05-22, distributed nationwide. Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of t
| Recall number | D-334-2013 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Performance Plus Marketing, Inc., Commerce, CA, United States |
| Recall initiated | 2012-12-17 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2013-11-14 |
| Distributed | Nationwide (US) |
| Quantity | 213,000 capsules |
| Reason classes | undeclared allergen, unapproved product |
| UPC / GTIN / UDI-DI | 00705105524764, 00736211123916, 00736211124012 |
| Lot numbers | 01/14, 01M0412, 04/15, 05M0412, 10M0412, 91782 |
Product
BLUE Diamond Pill, supplied in 1, 5 and 10 count blister packs, Male Sexual Enhancement, Distributed By: DH Distribution Los Angeles, CA 90026. 1 count blister: UPC 705105524764, 5 count blister: UPC 736211124012, 10 count blister: UPC 736211123916.
Reason for recall
Marketed Without an Approved NDA/ANDA: product may contain undeclared sildenafil, tadalafil and analogues of these FDA approved active ingredients, making them unapproved drugs
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-334-2013. 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.