# FDA recall D-0472-2022

> **Ultra Seal Corporation** · Class II · drug recall initiated 2022-01-24.

## Product

DBI 357 Super Magnum Quick Energy Stimulant (caffeine 200mg) tablets, packaged in a) 36-count bottles, b) 100-count bottles, c) 500-count bottles, and d) 3-count packets, Marketed by: DBI Distribution A Division of King Richard Promotions, Inc. P.O. Box 78546, Indianapolis, IN 46270

## Reason for recall

cGMP deviations

## Distribution

Nationwide within the United States

## Key facts

- **Recall number:** D-0472-2022
- **Recalling firm:** Ultra Seal Corporation
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2022-01-24
- **Report date:** 2022-02-09
- **Termination date:** 2023-10-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Paltz, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0472-2022

## Citation

> AI Analytics. FDA recall D-0472-2022. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0472-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
