Noven Pharmaceuticals recalls

Noven Pharmaceuticals has 51 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 27 Nov 2024. 12 are still ongoing. The most frequent reason is potency & assay.

Total recalls51since 2012
Last 12 months0reported
Class I00% of total
Ongoing12latest 27 Nov 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 50 98%Class III 1 2%

Why noven pharmaceuticals is recalled

By year

Ongoing noven pharmaceuticals recalls

12 active

All noven pharmaceuticals recalls, newest first

51 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIXelstrym (dextroamphetamine) transdermal system recalledXelstrymNoven PharmaceuticalsPackaging DefectsNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) CII, 20mg recalledDaytranaNoven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) CII, 15 mg recalledDaytranaNoven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) CII, 10mg recalledDaytranaNoven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) CII, 30 mg recalledDaytranaNoven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) recalledDaytranaNoven PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) Delivers recalledDaytranaNoven PharmaceuticalsOtherNationwide
DrugCLASS IIDaytrana (methylphenidate transdermal system) Delivers recalledDaytranaNoven PharmaceuticalsOtherNationwide
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.