US Drug Recall Register

FDA Drug Recalls

11,815 recalls · Class II, newest first

Class II · Moderate risk Terminated

PHENYLephrine HCl

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-901-01 D-0324-2022
Class II · Moderate risk Terminated

PHENYLephrine HCl

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-252-01 D-0323-2022
Class II · Moderate risk Terminated

Norepinephrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-926-01 D-0322-2022
Class II · Moderate risk Terminated

Norepinephrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-676-01 D-0321-2022
Class II · Moderate risk Terminated

Norepinephrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-651-01 D-0320-2022
Class II · Moderate risk Terminated

Norepinephrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-002-01 D-0319-2022
Class II · Moderate risk Terminated

Morphine Sulfate

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-427-01 D-0318-2022
Class II · Moderate risk Terminated

Fentanyl Citrate

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-327-02 D-0317-2022
Class II · Moderate risk Terminated

Fentanyl Citrate

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-327-01 D-0316-2022
Class II · Moderate risk Terminated

EPINEPHrine

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-027-01 D-0304-2022
Class II · Moderate risk Terminated

NOREPINEPHRINE 4 mg per 250 mL

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-451-01 D-0303-2022
Class II · Moderate risk Terminated

dilTIAZem HCl 125 mg per 125 mL

Reason Lack of Assurance of Sterility

SterRx, LLC NDC 70324-976-01 D-0302-2022