Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

1,969 recalls, newest first

Class II · Moderate risk

Estradiol Valerate 30 mg/ml

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-641-2013
Class II · Moderate risk

Estradiol Valerate 20 mg/ml

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-640-2013
Class II · Moderate risk

Estradiol Cypionate 5 mg/ml

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-639-2013
Class II · Moderate risk

Diazepam 5 mg/ml

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-638-2013
Class II · Moderate risk

Cyclosporine 2% ophthalmic

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-637-2013
Class II · Moderate risk

Cataract drops

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-635-2013
Class II · Moderate risk

Acetylcysteine 2 % Solution

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-634-2013
Class II · Moderate risk

Acetylcysteine 20 % solution

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes.

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-633-2013
Class II · Moderate risk

Acetylcysteine 10 % Solution

Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes

Terminated Sterility / contamination Clinical Specialties Compounding Pharmacy D-632-2013
Class III · Low risk

Disulfiram Tablets USP 250 mg

CGMP Deviation; cotton coil is missing in some packaged bottles

Terminated cGMP deviation Teva Pharmaceuticals USA, Inc. NDC 0093-5035-01 D-578-2013
Class III · Low risk

Tizanidine Tablets USP

Labeling Illegible: There is a possibility that the bottle labels do not contain the strength of the product as well as other printing details.

Terminated Labeling / mix-up Dr. Reddy'S Laboratories NDC 55111-180-15 D-238-2013
Class III · Low risk

Camila 0.35 mg Tablets

Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing

Terminated Chemical / undeclared Physicians Total Care, Inc. NDC 54868-4814-0 D-499-2013
Class III · Low risk

Oxcarbazepine Tablets

SubPotent Drug: The firm discovered out of specification results for assay and the extended investigation revealed the potential for lower weight tablets.

Terminated Wrong potency / content Boehringer Ingelheim Roxane Inc NDC 0054-0097-20 D-343-2014
Class II · Moderate risk

Donnatal Extentabs

Labeling: Incorrect or Missing Lot and/or Exp Date: Bottled product is labeled with an expiration date of Apr 2015. The correct expiration is Apr 2013.

Terminated Labeling / mix-up West-ward Pharmaceutical Corp. NDC 66213-421-10 D-306-2013
Class III · Low risk

Camila (norethindrone tablets, USP)

Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing

Terminated Chemical / undeclared Teva Pharmaceuticals USA, Inc. NDC 0555-0715-58 D-690-2013
Class III · Low risk

Errin (norethindrone tablets, USP)

Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing

Terminated Chemical / undeclared Teva Pharmaceuticals USA, Inc. NDC 0555-0344-58 D-689-2013
Class III · Low risk

Junel

Failed Impurity/Degradation Specification; an impurity identified as N-Butyl-Benzene Sulfonamide (NBBS) was detected during impurity testing

Terminated Chemical / undeclared Teva Pharmaceuticals USA, Inc. NDC 0555-9028-58 D-682-2013

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