Lanreotide recalls

The FDA has published 3 recalls involving Lanreotide since 2026. The latest was reported on 15 Apr 2026. Most were for sterility. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls3since 2026
Last 12 months3reported
Class I00% of total
Ongoing3latest 15 Apr 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why lanreotide is recalled

Companies

By year

Ongoing lanreotide recalls

3 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILanreotide Injection, 120 mg* recalled by Cipla USALanreotide AcetateCipla USASterilityNationwide
DrugCLASS IILanreotide Injection, 120 mg recalled by Cipla USALanreotide AcetateCipla USASterilityNationwide
DrugCLASS IILanreotide Injection, 120 mg/ per pre-filled syringe recalledLanreotide AcetateCipla USAParticulate MatterNationwide

All lanreotide recalls, newest first

3 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILanreotide Injection, 120 mg* recalled by Cipla USALanreotide AcetateCipla USASterilityNationwide
DrugCLASS IILanreotide Injection, 120 mg recalled by Cipla USALanreotide AcetateCipla USASterilityNationwide
DrugCLASS IILanreotide Injection, 120 mg/ per pre-filled syringe recalledLanreotide AcetateCipla USAParticulate MatterNationwide

Should you stop taking Lanreotide?

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.