Dermatone — Class II drug recall D-1242-2020
Terminated recall by Filltech USA, LLC, reported 2020-04-22, distributed nationwide. Microbial contamination of non-sterile products: positive test for yeast and bacteria.
| Recall number | D-1242-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Filltech USA, LLC, Rockwell, NC, United States |
| Recall initiated | 2020-03-19 |
| Classified | 2020-04-16 |
| Reported by FDA | 2020-04-22 |
| Terminated | 2022-01-14 |
| Distributed | Nationwide (US) |
| Reason classes | microbial contamination, sterility |
| Pathogens | yeast |
| UPC / GTIN / UDI-DI | 00087052727338, 00087052727345 |
Product
Dermatone (avobenzone, homosalate, octisalate, and octocrylene) Sunscreen Lotion Fragrance Free, SPF 50, packaged in a) 1.5 fl. oz. (44 mL) tottles, UPC: 087052727338; b) 2 Fl. OZ. (59 mL) tubes, UPC: 08705272732; c) 4 FL. OZ. (118 mL) tubes, UPC: 087052727345, Distributed By: Beaumont Products, Inc. Kennesaw, GA 30144
Reason for recall
Microbial contamination of non-sterile products: positive test for yeast and bacteria.
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-1242-2020. 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.