# FDA recall D-0027-2019

> **Product Quest Manufacturing LLC** · Class II · drug recall initiated 2018-08-03.

## Product

DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Distributed by: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 0 20908 05100 3.

## Reason for recall

Microbial Contamination of Non-Sterile Products: sample tested positive for Staphylococcus aureus.

## Distribution

Nationwide in the USA

## Key facts

- **Recall number:** D-0027-2019
- **Recalling firm:** Product Quest Manufacturing LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2018-08-03
- **Report date:** 2018-10-24
- **Termination date:** 2021-03-30

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0027-2019

## Citation

> AI Analytics. FDA recall D-0027-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/D-0027-2019. Source: US FDA. Licensed CC0.

---

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