US Drug Recall Register

FDA Drug Recalls

14,450 recalls · Class II, newest first

Class II · Moderate risk Terminated

Doxazosin Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-415-01 D-0389-2023
Class II · Moderate risk Terminated

Doxazosin Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-213-01 D-0388-2023
Class II · Moderate risk Terminated

Doxazosin Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-414-01 D-0387-2023
Class II · Moderate risk Terminated

Doxazosin Tablets USP 1 mg

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-211-01 D-0386-2023
Class II · Moderate risk Terminated

Dofetilide Capsules 500 mcg

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-492-12 D-0385-2023
Class II · Moderate risk Terminated

Dofetilide Capsules 250 mcg

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-491-12 D-0384-2023
Class II · Moderate risk Terminated

Dofetilide Capsules

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-490-12 D-0383-2023
Class II · Moderate risk Terminated

Daptomycin for Injection 500 mg per vial

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-435-05 D-0382-2023
Class II · Moderate risk Terminated

Daptomycin for Injection 350 mg/vial

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-434-05 D-0381-2023
Class II · Moderate risk Terminated

Clopidogrel Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-218-10 D-0380-2023
Class II · Moderate risk Terminated

BusPIRone Hydrochloride Tablets USP 30 mg

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-289-12 D-0379-2023
Class II · Moderate risk Terminated

BusPIRone Hydrochloride Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-202-16 D-0378-2023
Class II · Moderate risk Terminated

BusPIRone Hydrochloride Tablets USP 15 mg

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-203-01 D-0377-2023
Class II · Moderate risk Terminated

BusPIRone Hydrochloride Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-200-01 D-0376-2023
Class II · Moderate risk Terminated

BusPIRone Hydrochloride Tablets USP 7.5 mg

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-201-01 D-0375-2023
Class II · Moderate risk Terminated

Atorvastatin Calcium Tablets USP

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-044-15 D-0371-2023
Class II · Moderate risk Terminated

Aripiprazole Tablets

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-283-10 D-0370-2023
Class II · Moderate risk Terminated

Aripiprazole Tablets

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-282-10 D-0369-2023
Class II · Moderate risk Terminated

Aripiprazole Tablets

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-281-10 D-0368-2023
Class II · Moderate risk Terminated

Aripiprazole Tablets

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-280-10 D-0367-2023
Class II · Moderate risk Terminated

Aripiprazole Tablets

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-279-10 D-0366-2023
Class II · Moderate risk Terminated

Aripiprazole Tablets

Reason CGMP Deviations: recalling drug products following an FDA inspection.

Accord Healthcare, Inc. NDC 16729-278-10 D-0365-2023