# FDA recall D-1150-2023

> **APG SEVEN, INC** · Class I · drug recall initiated 2023-08-03.

## Product

Vegetal Vigra, 200mg capsules, 8-count bottle, Manufacturer: Hand-shaking (Int'l) Corp. USA ADD: Hand-shaking Mansion, the 5th Ave., Stanford, USA. UPC 8 931028 556885

## Reason for recall

Marketed Without an Approved NDA/ANDA: FDA analysis found the product to be tainted with sildenafil an ingredient found in a FDA approved product for the treatment of male sexual enhancement, making this an unapproved drug.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-1150-2023
- **Recalling firm:** APG SEVEN, INC
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2023-08-03
- **Report date:** 2023-09-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Miami, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1150-2023

## Citation

> AI Analytics. FDA recall D-1150-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1150-2023. Source: US FDA. Licensed CC0.

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