ProRx LLC recalls

ProRx LLC recalls Semaglutide Injection, 5 mg/2 mL (2.5 mg/mL), 2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619

ProRx recalls Semaglutide injections due to lack of sterility assurance. Affected units have NDC 84139-225-02 and lot PRORX052125-4. No remedy specified in recall notice.

ProRx LLC recalls Tirzepatide Injection, 27 mg/3 mL (9 mg/mL), 3mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619

ProRx recalls 27mg/3mL Tirzepatide injection vials due to lack of sterility assurance. This could lead to infections if used improperly. Affected vials have NDC 84139-209-03 and lot PRORX08062025-3.

ProRx LLC recalls Semaglutide Injection, 8mg/3.2mL (2.5 mg/mL), 3.2mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619

ProRx recalls Semaglutide injections with potential lack of sterility assurance. Affected lots from May 2025 production. Consumers should contact ProRx for details.

ProRx LLC recalls Semaglutide Injection, 10 mg/4 mL (2.5 mg/mL), 4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619

ProRx recalls Semaglutide injections with potential contamination risk. Affected lots have specific batch numbers and expiration dates. Consumers should contact ProRx for details.

ProRx LLC recalls SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC

ProRx recalls compounded SEMAGLUTIDE 10mg/4mL vials due to lack of sterility assurance. Affected units have NDC 84139-225-04 and were compounded by ProRx in Exton, PA. No remedy specified in recall notice.

ProRx LLC recalls TIRZEPATIDE 20 mg/2mL (10/mg/mL), Rx Only, 2mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-01

ProRx LLC recalls TIRZEPATIDE 60 mg/3mL (20/mg/mL), Rx Only, 3mL Multiple Dose Vial, Mfd by: ProRx Exton, PA, 19341, NDC 84139-210-02

ProRx recalls TIRZEPATIDE 60mg/3mL vials due to lack of sterility assurance. Affected vials have specific lot numbers and expiration dates. Consumers should contact ProRx for details.

ProRx LLC recalls SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton,

ProRx recalls SEMAGLUTIDE 5mg/2mL compounded vials due to lack of sterility assurance. Affected vials have specific lot numbers and expiration dates. Consumers should contact ProRx for details.

ProRx LLC recalls Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX

ProRx recalls Semaglutide/Cyanocobalamin injection vials with potential contamination. Affected vials have NDC 84139-225-02 and Lot # ProRx031924-1. Consumers should contact ProRx for details.

ProRx LLC recalls Semaglutide, 2 mL (2.5mg/mL), Compounded RX Product, Multidose SC inj, glass vial, ProRx, 267-565-7008, NDC 84139-225-01