Semaglutide recalls

The FDA has published 38 recalls involving Semaglutide since 2021. The latest was reported on 19 Aug 2026. Most were for sterility. Apollo Care 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 recalls38since 2021
Last 12 months19reported
Class I00% of total
Ongoing32latest 19 Aug 2026

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 38 100%Class III 0 0%

By year

Ongoing semaglutide recalls

32 active

All semaglutide recalls, newest first

38 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IISemaglutide 5mg (1mg/mL), Glycine 25 mg recalled by Apollo CareApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 4.5mg (0.9 mg/mL) Sterile Multi-Dose Vial recalledApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 9mg (4.5 mg/mL) Sterile Multi-Dose Vial recalledApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 10mg (5mg/mL), Glycine 10 mg recalled by Apollo CareApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 20mg (5mg/mL), Glycine 20 mg recalled by Apollo CareApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 0.9mg (0.9 mg/mL) Sterile Multi-Dose Vial recalledApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 6.75mg (4.5 mg/mL) Sterile Multi-Dose Vial recalledApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 2.5mg (1mg/mL), Glycine 12.5 mg recalled by Apollo CareApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 2.25MG (0.9 mg/mL) Sterile Multi-Dose Vial recalledApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 12.5MG (2.5MG/mL) Sterile Multi-Dose Vial recalledApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide 7.5mg (5mg/mL), Glycine 7.5 mg recalled by Apollo CareApollo CareParticulate MatterNationwide
DrugCLASS IISemaglutide Injection, 5 mg/ (2.5 mg/mL) Multidose Vial recalledProRxSterilityTX, UT
DrugCLASS IISemaglutide Injection (2.5 mg/mL) Multidose Vial recalled by ProRxProRxSterilityTX, UT
DrugCLASS IISemaglutide Injection, 8mg/ (2.5 mg/mL) Multidose Vial recalled by ProRxProRxSterilityTX, UT
DrugCLASS IISemaglutide Injection, 2.5mg/ (2.5 mg/mL) Multidose Vial recalledProRxSterilityTX, UT
DrugCLASS IISemaglutide Injection, 6mg/ (2.5 mg/mL) Multidose Vial recalled by ProRxProRxSterilityTX, UT
DrugCLASS IISemaglutide Injection, 10 mg/ (2.5 mg/mL) Multidose Vial recalledProRxSterilityTX, UT
DrugCLASS IISemaglutide with B12 for Injection, all strengths recalled by GenoGenixGenoGenixSterilityNationwide
DrugCLASS IISemaglutide for Injection, a) 20 mg b) 20 mg/mL Multi-Dose recalledGenoGenixSterilityNationwide
DrugCLASS IISemaglutide, 2.5 mg/mL injection, Boothwyn Pharmacy recalledBoothwyn PharmacyPotency & AssayNationwide
DrugCLASS IISemaglutide, 2.5 mg/mL injection, Boothwyn Pharmacy recalledBoothwyn PharmacyPotency & AssayNationwide
DrugCLASS IISemaglutide, 2.5 mg/mL injection, Boothwyn Pharmacy recalledBoothwyn PharmacyPotency & AssayNationwide
DrugCLASS IISemaglutide/Cyanocobalamin Injectable, 5mg/1mg/mL recalledThrive Health and Wellness, LLCSterilityNationwide
DrugCLASS IISemaglutide, 2.5 mg/mL, pre-filled syringe recalledThrive Health and Wellness, LLCSterilityNationwide
DrugCLASS IISemaglutide, 5 mg/mL, pre-filled syringe recalledThrive Health and Wellness, LLCSterilityNationwide
DrugCLASS IISemaglutide 10mg/ (2.5mg/mL) Multiple Dose Vial recalled by ProRxProRxSterilityNationwide
DrugCLASS IISemaglutide 5mg/ (2.5mg/mL) recalled by ProRxProRxSterilityNationwide
DrugCLASS IISemaglutide / Cyanocobalamin Injection recalled by ProRxProRxSterilityNationwide
DrugCLASS IISemaglutide (2.5mg/mL), Compounded RX Product recalled by ProRxProRxSterilityNationwide
DrugCLASS IISemaglutide/Cyanocobalamin 2mg/0.4mg/mL, 1mLvials recalledTMC AcquisitionsSterilityNationwide

Should you stop taking Semaglutide?

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.