Lansoprazole recalls

The FDA has published 15 recalls involving Lansoprazole since 2013. The latest was reported on 17 Apr 2024. Most were for potency & assay. Zydus Pharmaceuticals has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls15since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 17 Apr 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 13 87%Class III 2 13%

By year

All lansoprazole recalls, newest first

15 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILansoprazole Delayed-Release Capsules USP, 15 mg recalledNatco PharmaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILansoprazole Delayed-Release Capsules USP, 15 mg recalledNatco PharmaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILansoprazole Delayed-Release Capsules, USP, 15 mg, a) recalledLansoprazoleDr. Reddy's LaboratoriesPotency & AssayNationwide
DrugCLASS IILansoprazole Delayed-Release Capsules, USP, 30 mg recalledLansoprazoleDr. Reddy's LaboratoriesPotency & AssayNationwide
DrugCLASS IILansoprazole Delayed-Release Orally Disintegrating Tablets recalledLansoprazoleZydus PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILansoprazole Delayed-Release Orally Disintegrating Tablets recalledLansoprazoleZydus PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILansoprazole Delayed-Release Orally Disintegrating Tablets recalledLansoprazoleZydus PharmaceuticalsPotency & AssayNationwide
DrugCLASS IILansoprazole Delayed-Release Orally Disintegrating Tablets recalledLansoprazoleZydus PharmaceuticalsPotency & AssayNationwide
DrugCLASS IIILansoprazole Delayed-Release Orally Disintegrating Tablets recalledLansoprazoleTeva Pharmaceuticals USAPotency & AssayNationwide
DrugCLASS IIILansoprazole Delayed-Release Capsules, USP, 30 mg recalledMckesson Packaging ServicesLabeling ErrorsNationwide
DrugCLASS IILansoprazole Delayed-Release Capsules recalled by Wockhardt UsaWockhardt UsaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILansoprazole Delayed-Release Capsules recalled by Wockhardt UsaWockhardt UsaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILansoprazole Delayed-Release Capsules, USP, For Repackaging Only recalledWockhardt UsaManufacturing (CGMP) DeviationsNationwide
DrugCLASS IILansoprazole 3 mg/mL Susp, Health Innov Pharmacy recalledHealth Innovations PharmacySterilityNC
DrugCLASS IILansoprazole Delayed-release Capsules recalled by Mylan PharmaceuticalsLansoprazoleMylan PharmaceuticalsOtherNationwide

Should you stop taking Lansoprazole?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.