NATURECT Capsules Dietary Supplement 500 mg — Class I drug recall D-1346-2014
Terminated recall by Tendex, reported 2014-05-28, distributed nationwide. Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient,
| Recall number | D-1346-2014 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tendex, Beverly Hills, CA, United States |
| Recall initiated | 2013-11-19 |
| Classified | 2014-05-21 |
| Reported by FDA | 2014-05-28 |
| Terminated | 2014-09-18 |
| Distributed | Nationwide (US) |
| Reason classes | undeclared allergen, unapproved product |
| UPC / GTIN / UDI-DI | 00893020242013, 00893020242051, 00893020242105, 00893020242204, 00893020242402 |
| Lot numbers | 07/16, F51Q |
Product
NATURECT Capsules Dietary Supplement 500 mg, supplied in 1 count blister pack and 5, 10, 20, and 40- count bottles, Distributed by P-Boost, Los Angeles, CA 900466
Reason for recall
Marketed Without an Approved NDA/ANDA: FDA analysis found the product to contain undeclared active ingredient, tadalafil, thus making these products 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-1346-2014. 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.