Class II · Moderate risk Ongoing
UltraSure Anti-Perspirant & Deodorant
Reason CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
Dryses Aluminum Chlorohydrate Antiperspirant Solution
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
cGMP Deviations; product does not comply with cGMP requirements
What was recalled
Dryses Aluminum Chlorohydrate Antiperspirant Solution, 3.4 fl. oz (100 mL) bottle, over the counter, Manufactured by Sesderma S.L., Valencia, Spain, NDC 63181-0015-1, UPC 8 470003 244268
- Recalling firm
- Sesderma, SL
- NDC code
- 63181-0015-1
- Origin
- N/A, Spain
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0842-2016
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
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Class II · Moderate risk Ongoing
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