# FDA recall D-0573-2023

> **Gadget Island, Inc** · Class I · drug recall initiated 2023-04-26.

## Product

DYNAMITE SUPER capsule, 58,000 MG, 1-count blister card, Made in America, UPC 6 75799 37602 7.

## Reason for recall

Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

## Distribution

Nationwide in the USA.

## Key facts

- **Recall number:** D-0573-2023
- **Recalling firm:** Gadget Island, Inc
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2023-04-26
- **Report date:** 2023-05-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** West Sacramento, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0573-2023

## Citation

> AI Analytics. FDA recall D-0573-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/D-0573-2023. Source: US FDA. Licensed CC0.

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