Ceftriaxone recalls

The FDA has published 22 recalls involving Ceftriaxone since 2014. The latest was reported on 24 May 2023. Most were for sterility. Astral SteriTech Private 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 recalls22since 2014
Last 12 months0reported
Class I523% of total
Ongoing0latest 24 May 2023

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 5 23%Class II 11 50%Class III 6 27%

By year

All ceftriaxone recalls, newest first

22 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IICeftriaxone for Injection, USP per Pharmacy recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP 250 mg per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP 500 mg per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP 250 mg per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP 500 mg per vial recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS IICeftriaxone for Injection, USP per Pharmacy recalledAstral SteriTech PrivateSterilityNationwide
DrugCLASS ICeftriaxone for Injection recalled by Lupin PharmaceuticalsLupin PharmaceuticalsParticulate MatterNationwide
DrugCLASS ICeftriaxone for Injection recalled by Lupin PharmaceuticalsLupin PharmaceuticalsParticulate MatterNationwide
DrugCLASS ICeftriaxone for Injection USP, 500 mg recalled by Lupin PharmaceuticalsLupin PharmaceuticalsParticulate MatterNationwide
DrugCLASS ICeftriaxone for Injection USP, 250 mg recalled by Lupin PharmaceuticalsLupin PharmaceuticalsParticulate MatterNationwide
DrugCLASS IIICeftriaxone for Injection, USP use Vials recalled by SandozCeftriaxone SodiumSandozLabeling ErrorsWI
DrugCLASS IIICeftriaxone for Injection USP, 250mg/vial recalledAidarex PharmaceuticalsPotency & AssayGA, IN
DrugCLASS IIICeftriaxone for Injection USP, 250 mg, Single Use Vial recalledLupin PharmaceuticalsManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIICeftriaxone for Injection USP, Single Use Vial recalledLupin PharmaceuticalsManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIICeftriaxone for Injection USP, 500 mg, Single Use Vial recalledLupin PharmaceuticalsManufacturing (CGMP) DeviationsNationwide
DrugCLASS IIICeftriaxone for Injection USP, Single Use Vial recalledLupin PharmaceuticalsManufacturing (CGMP) DeviationsNationwide
DrugCLASS IICeftriaxone Sodium 2000mg / NS, Qty:4 recalled by LincareLincareSterilityAR
DrugCLASS ICeftriaxone for Injection and Dextrose Injection in Duplex Container recalledB. Braun MedicalParticulate MatterNationwide

Should you stop taking Ceftriaxone?

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.