US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class II · Moderate risk Terminated

Cyanocobalamin Injection

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0330-3 D-0948-2020
Class II · Moderate risk Terminated

Coenzyme Q10 Injection

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0411-1 D-0947-2020
Class II · Moderate risk Terminated

Calcium Chloride Injection

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0225-3 D-0946-2020
Class II · Moderate risk Terminated

Biotin

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0220-3 D-0945-2020
Class II · Moderate risk Terminated

Betamethasone Acetate/Betamethasone

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0621-5 D-0944-2020
Class II · Moderate risk Terminated

Betamethasone Acetate/Betamethasone

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0621-1 D-0943-2020
Class II · Moderate risk Terminated

Betamethasone Acetate/Betamethasone

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0620-2 D-0942-2020
Class II · Moderate risk Terminated

B-Complex 110 Injectable

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0212-3 D-0941-2020
Class II · Moderate risk Terminated

AscorbiX

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0226-5 D-0940-2020
Class II · Moderate risk Terminated

AscorbiX

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0226-3 D-0939-2020
Class II · Moderate risk Terminated

Alprostadil

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0543-2 D-0936-2020
Class II · Moderate risk Terminated

Alprostadil

Reason Lack of Assurance of Sterility

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical NDC 71283-0538-2 D-0935-2020
Class II · Moderate risk Terminated

Ranitidine 300 mg

Reason CGMP Deviations: Presence of NDMA impurity detected in product.

Direct Rx NDC 61919-455-30 D-0017-2021
Class II · Moderate risk Terminated

Ranitidine 150 mg

Reason CGMP Deviations: Presence of NDMA impurity detected in product.

Direct Rx NDC 61919-339-60 D-0016-2021
Class II · Moderate risk Terminated

Ranitidine Hydrochloride

Reason CGMP Deviations: Presence of NDMA impurity detected in product.

Spectrum Laboratory Products D-0825-2020
Class II · Moderate risk Terminated

Nystatin Oral Suspension

Reason Subpotent: Out of specification for assay at the 12-month time point.

Pharmaceutical Associates Inc NDC 0121-0810-16 D-0824-2020
Class III · Low risk Terminated

methylPREDNISolone Sodium Succinate For Injection

Reason Labeling: Incorrect Instructions: Vial label incorrectly instructs healthcare professional to reconstitute product with 16 mL rather than the correct volume of 8 mL of Bacteriostatic Water for Injection with Benzyl Alcohol.

Hikma Pharmaceuticals USA Inc. NDC 0143-9850-01 D-0801-2020
Class II · Moderate risk Terminated

Testosterone Cypionate for Injection

Reason cGMP Deviations; released lots were manufactured under similar manufacturing conditions to a previously rejected OOS Lot.

Sun Pharmaceutical Industries, Inc. NDC 62756-015-40 D-0788-2020
Class II · Moderate risk Terminated

Testosterone Cypionate for Injection

Reason cGMP Deviations; released lots were manufactured under similar manufacturing conditions to a previously rejected OOS Lot.

Sun Pharmaceutical Industries, Inc. NDC 62756-017-40 D-0787-2020
Class II · Moderate risk Terminated

ranitidine hydrochloride

Reason CGMP Deviations: Received notice from supplier of potential -Nitrosodimethylamine (NDMA) amounts above established levels.

PD-Rx Pharmaceuticals, Inc. NDC 43063-844-14 D-0826-2020