RecallRadar

FDA Drug recall D-0337-2021

Estradiol Transdermal System Delivers 0.0375 mg/day, 8 Systems/box, Rx only, Mfd. by: Noven Pharmaceuticals, Inc

On 2021-04-28 the FDA classified a Class II recall of Estradiol Transdermal System Delivers 0.0375 mg/day, 8 Systems/box, Rx only, Mfd. by: Noven Pharmaceuticals, Inc by Noven Pharmaceuticals, citing defective Delivery System: Out of specification for release rate testing and shear, an attribute related to the adhesive properties of the transdermal patches. As a result, patien….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0337-2021
ClassificationClass II
Statusterminated
Initiated2021-04-16
Published2021-04-28
Last updated2026-09-13 11:52 UTC
CompanyNoven Pharmaceuticals
DistributionUS

Product

Estradiol Transdermal System Delivers 0.0375 mg/day, 8 Systems/box, Rx only, Mfd. by: Noven Pharmaceuticals, Inc. Miami, Florida 33186 Dist. by: Noven Therapeutics, LLC Miami, Florida 33186, NDC 68968-3437-8

Reason

Defective Delivery System: Out of specification for release rate testing and 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.

Identifiers

ndc68968-3425-8
ndc68968-3437-8
ndc68968-3450-8
ndc68968-3475-8
ndc68968-3410-8
code_infoLot #: 88321 Exp. 02/2022

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0337-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.