Lupin Somerset recalls

Lupin Somerset has 13 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 1 May 2019. The most frequent reason is potency & assay.

Total recalls13since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 1 May 2019

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 5 38%Class III 8 62%

Why lupin somerset is recalled

By year

All lupin somerset recalls, newest first

13 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIMorphine Sulfate Extended-Release Tablets, 30 mg recalledMorphine SulfateLupin SomersetPotency & AssayNationwide
DrugCLASS IIIMorphine Sulfate Extended-Release Tablets, 15 mg recalledMorphine SulfateLupin SomersetPotency & AssayNationwide
DrugCLASS IIIMorphine Sulfate Extended-Release Tablets, 200 mg recalledMorphine SulfateLupin SomersetPotency & AssayNationwide
DrugCLASS IIIMorphine Sulfate Extended-Release Tablets, 100 mg recalledMorphine SulfateLupin SomersetPotency & AssayNationwide
DrugCLASS IIIMorphine Sulfate Extended-Release Tablets, 60 mg recalledMorphine SulfateLupin SomersetPotency & AssayNationwide
DrugCLASS IIGavilyte-N, PEG-3350, Sodium chloride recalled by Lupin SomersetGavilyte-nLupin SomersetOtherNationwide
DrugCLASS IIFluocinolone Acetonide Topical Solution, USP, 0.01 % recalledFluocinolone AcetonideLupin SomersetPotency & AssayNationwide
DrugCLASS IINitrofurantoin Oral Suspension, USP, 25mg recalled by Lupin SomersetNitrofurantoinLupin SomersetPotency & AssayNationwide
DrugCLASS IIFluocinolone Acetonide Topical Solution recalled by Lupin SomersetFluocinolone AcetonideLupin SomersetPotency & AssayNationwide
DrugCLASS IIIMorphine Sulfate Extended-Release Tablets, 30 mg recalledMorphine SulfateLupin SomersetPotency & AssayNationwide
DrugCLASS IINitrofurantoin Oral Suspension USP, 25mg recalled by Lupin SomersetNitrofurantoinLupin SomersetPotency & AssayNationwide
DrugCLASS IIIEquate ClearLAX, Polyethylene Glycol 3350 Powder recalledLupin SomersetPackaging DefectsNationwide
DrugCLASS IIIHydrocodone Bitartrate and Acetaminophen Tablets, USP, 5 mg/325 mg recalledHydrocodone Bitartrate And AcetaminophenLupin SomersetLabeling ErrorsOH

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.