Cipla USA recalls

Cipla USA has 23 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 8 Jul 2026. 21 are still ongoing. 17 were reported in the last 12 months. The most frequent reason is nitrosamine impurity.

Total recalls23since 2023
Last 12 months17reported
Class I14% of total
Ongoing21latest 8 Jul 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 1 4%Class II 18 78%Class III 4 17%

By year

Ongoing cipla usa recalls

21 active

All cipla usa recalls, newest first

23 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IICinacalcet Hydrochloride Tablets, 60 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 90 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 30 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 60 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 90 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 30 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IILanreotide Injection, 120 mg* recalled by Cipla USALanreotide AcetateCipla USASterilityNationwide
DrugCLASS IILanreotide Injection, 120 mg recalled by Cipla USALanreotide AcetateCipla USASterilityNationwide
DrugCLASS IIINilotinib Capsules recalled by Cipla USANilotinibCipla USAPotency & AssayNationwide
DrugCLASS IIINilotinib Capsules recalled by Cipla USANilotinibCipla USAPotency & AssayNationwide
DrugCLASS IIIDiclofenac Sodium Topical Gel recalled by Cipla USADiclofenac SodiumCipla USAOtherNationwide
DrugCLASS IILanreotide Injection, 120 mg/ per pre-filled syringe recalledLanreotide AcetateCipla USAParticulate MatterNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 60 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IILanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum CarbonateCipla USAPotency & AssayNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 30 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IICinacalcet Hydrochloride Tablets, 90 mg recalled by Cipla USACinacalcetCipla USANitrosamine ImpurityNationwide
DrugCLASS IILanthanum Carbonate chewable tablets, 1000mg* recalled by Cipla USALanthanum CarbonateCipla USAPotency & AssayNationwide
DrugCLASS IIIAlbuterol Sulfate, Inhalation Aerosol, 90 mcg recalled by Cipla USAAlbuterol SulfateCipla USAPotency & AssayNationwide
DrugCLASS IIBudesonide Inhalation Suspension, 0.5mg/-dose ampules per, five recalledBudesonideCipla USASterilityNationwide
DrugCLASS IILanthanum Carbonate Chewable Tablets, 1000mg recalled by Cipla USACipla USAOtherNationwide
DrugCLASS IILanthanum Carbonate Chewable Tablets, 1000mg recalled by Cipla USACipla USAOtherNationwide
DrugCLASS IIIpratropium Bromide and Albuterol Sulfate Inhalation recalledIpratropium Bromide And Albuterol SulfateCipla USAPackaging DefectsNationwide
DrugCLASS IAlbuterol Sulfate Inhalation Aerosol, 90 mcg recalled by Cipla USAAlbuterol SulfateCipla USAPackaging DefectsNationwide

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.