US Drug Recall Register

FDA Drug Recalls

14,801 recalls, newest first

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
Class III · Low risk Terminated

Fexofenadine HCl

Reason Failed dissolution specifications

Dr. Reddy's Laboratories, Inc. NDC 43598-823-31 D-0275-2022
Class III · Low risk Terminated

Allergy Relief D Fexofenadine HCl

Reason Failed dissolution specifications

Dr. Reddy's Laboratories, Inc. NDC 49035-273-30 D-0274-2022
Class III · Low risk Terminated

Allergy Relief D Fexofenadine HCl

Reason Failed dissolution specifications

Dr. Reddy's Laboratories, Inc. NDC 69842-249-30 D-0273-2022
Class III · Low risk Terminated

Antihistamine & Nasal Decongestant

Reason Failed dissolution specifications

Dr. Reddy's Laboratories, Inc. NDC 0638-1242-07 D-0271-2022
Class III · Low risk Terminated

Antihistamine & Nasal Decongestant

Reason Failed dissolution specifications

Dr. Reddy's Laboratories, Inc. NDC 0536-1242-34 D-0270-2022