DERMATONE — Class II drug recall D-0027-2019
Terminated recall by Product Quest Manufacturing LLC, reported 2018-10-24, distributed nationwide. Microbial Contamination of Non-Sterile Products: sample tested positive for Staphylococcus aureus.
| Recall number | D-0027-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Product Quest Manufacturing LLC, Daytona Beach, FL, United States |
| Recall initiated | 2018-08-03 |
| Classified | 2018-10-16 |
| Reported by FDA | 2018-10-24 |
| Terminated | 2021-03-30 |
| Distributed | Nationwide (US) |
| Quantity | 5,025 sticks |
| Reason classes | microbial contamination, sterility |
| Pathogens | staphylococcus |
| UPC / GTIN / UDI-DI | 00020908051003 |
| Lot numbers | 172428G |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0027-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.