# FDA recall D-1346-2014

> **Tendex** · Class I · drug recall initiated 2013-11-19.

## 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.

## Distribution

Nationwide.

## Key facts

- **Recall number:** D-1346-2014
- **Recalling firm:** Tendex
- **Classification:** Class I
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-11-19
- **Report date:** 2014-05-28
- **Termination date:** 2014-09-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Beverly Hills, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1346-2014

## Citation

> AI Analytics. FDA recall D-1346-2014. Retrieved 2026-05-29 from https://api.ai-analytics.org/recall/D-1346-2014. Source: US FDA. Licensed CC0.

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