DERMATONE No-Touch Sunscreen Stick recalled over sterility concerns
- Recall date
- August 3, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Product Quest Manufacturing LLC recalls DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Dis…
- Recall number
- D-0027-2019
- FDA classification
- Class II
- Brand / firm
- Product Quest Manufacturing LLC
- Sold / distributed
- Nationwide in the USA
Why it was recalled
Microbial Contamination of Non-Sterile Products: sample tested positive for Staphylococcus aureus.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
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.
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