Combipatch (estradiol/norethindrone Acetate Transdermal System) recalls

Combipatch (estradiol/norethindrone Acetate Transdermal System) products have been recalled 2 times, most recently on 25 Aug 2021. The recalling company is usually Noven Pharmaceuticals. The most common reason is potency & assay.

Total recalls2since 2021
Last 12 months0reported
Class I00% of total
Ongoing2latest 25 Aug 2021

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why combipatch (estradiol/norethindrone acetate transdermal system) is recalled

Companies

Product types

By year

Ongoing combipatch (estradiol/norethindrone acetate transdermal system) recalls

2 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IICombipatch (estradiol/norethindrone acetate transdermal recalledCombipatch (estradiol/norethindrone Acetate Transdermal System)Noven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IICombipatch (estradiol/norethindrone acetate transdermal recalledCombipatch (estradiol/norethindrone Acetate Transdermal System)Noven PharmaceuticalsPotency & AssayNationwide

All combipatch (estradiol/norethindrone acetate transdermal system) recalls, newest first

2 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IICombipatch (estradiol/norethindrone acetate transdermal recalledCombipatch (estradiol/norethindrone Acetate Transdermal System)Noven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IICombipatch (estradiol/norethindrone acetate transdermal recalledCombipatch (estradiol/norethindrone Acetate Transdermal System)Noven PharmaceuticalsPotency & AssayNationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.