Home Recalls D-0485-2015
Class II · Moderate risk Terminated Initiated Feb 25, 2015 (12 years ago)
Minivelle (estradiol transdermal system) 0.05 mg/day, 8-count box, Rx only, Manufactured…
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Temperature Abuse: Prolonged exposure to temperatures outside of labeled storage conditions.
What was recalled
Minivelle (estradiol transdermal system) 0.05 mg/day, 8-count box, Rx only, Manufactured by Noven Pharmaceuticals, Inc., Miami, Florida 33186, Distributed by Noven Pharmaceuticals, LLC, Miami, Florida 33186, NDC 68968-6650-8
Recalling firm Noven Pharmaceuticals, Inc.
NDC code 68968-6650-8
Origin FL, United States
Initiated by Voluntary: Firm initiated
FDA recall number D-0485-2015
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 Jan 26, 2026
Reason Presence of Foreign substance - potential presence of metal particulate matter
Class II · Moderate risk Ongoing Jan 26, 2026
Reason Presence of Foreign substance - potential presence of metal particulate matter