US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 4, 2018 (8 years ago)

Minivelle (estradiol transdermal system) 0.0375 mg/day, 1 System per pouch (NDC…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Defective Delivery System: no longer meets the specification for shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patients could experience patches that do not stick well to the skin.

What was recalled

Minivelle (estradiol transdermal system) 0.0375 mg/day, 1 System per pouch (NDC 68968-6637-1), packaged in 8 pouches per box (NDC 68968-6637-8), Rx only, Mfd. by: Noven Pharmaceuticals, Inc., Miami, Florida 33186; Dist. by: Noven Therapeutics, LLC, Miami, Florida 33186.

Recalling firm
Noven Pharmaceuticals, Inc.
NDC code
68968-6637-1
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0863-2018

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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