# FDA recall D-0572-2018

> **A&H Focal Inc.** · Class II · drug recall initiated 2017-03-07.

## Product

Tiger King tablets, labeling is in foreign language

## Reason for recall

Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.

## Distribution

NY and NJ through six retail stores named "Asian Food Markets"

## Key facts

- **Recall number:** D-0572-2018
- **Recalling firm:** A&H Focal Inc.
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2017-03-07
- **Report date:** 2018-02-07
- **Termination date:** 2019-06-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Staten Island, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0572-2018

## Citation

> AI Analytics. FDA recall D-0572-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/D-0572-2018. Source: US FDA. Licensed CC0.

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