US Drug Recall Register

FDA Drug Recalls

17,898 recalls, newest first

Class II · Moderate risk Terminated

*Mitomycin 0.04% Ophth DR eye drops

Reason Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Medical Center Pharmacy, Inc. NDC 67457-0518-05 D-1077-2020
Class II · Moderate risk Terminated

C-*Gentamicin/Bacitracin Bladder Irrigation in N.S.

Reason Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Medical Center Pharmacy, Inc. NDC 63323-0010-02 D-1076-2020
Class II · Moderate risk Terminated

*Morphine 2 mg/mL Cassette

Reason Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Medical Center Pharmacy, Inc. NDC 00409-1134-03 D-1075-2020
Class II · Moderate risk Terminated

C-*Vancomycin Opthal 14 mg drops

Reason Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Medical Center Pharmacy, Inc. NDC 67457-0340-01 D-1074-2020
Class II · Moderate risk Terminated

C-*Albumin Eye Drop 10% S

Reason Lack of Assurance of Sterility: due to concerns with production processes which cannot assure sterility of products intended to be sterile.

Medical Center Pharmacy, Inc. NDC 44206-0251-05 D-1073-2020
Class II · Moderate risk Terminated

Doxycycline Capsules

Reason CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.

Sun Pharmaceutical Industries, Inc. NDC 63304-616-50 D-1033-2020
Class II · Moderate risk Terminated

Doxycycline Capsules

Reason CGMP Deviations: Doxycycline capsules were not manufactured under Current Good Manufacturing Practice conditions.

Sun Pharmaceutical Industries, Inc. NDC 63304-615-01 D-1032-2020
Class II · Moderate risk Terminated

Pantoprazole Sodium Delayed-Release Tablets

Reason CGMP Deviations: Presence of dark brown discoloration on edges of tablets

Jubilant Cadista Pharmaceuticals, Inc. NDC 59746-284-90 D-1058-2020
Class II · Moderate risk Terminated

Levonorgestrel and Ethinyl Estradiol Tablets USP

Reason Failed Content Uniformity Specifications: Out Of Specification test results observed for content uniformity.

Lupin Pharmaceuticals Inc. NDC 68180-857-11 D-1056-2020
Class III · Low risk Terminated

Bekyree

Reason Failed Content Uniformity Specifications: Out Of Specification test results observed for content and blend uniformity.

Lupin Pharmaceuticals Inc. NDC 68180-879-11 D-1055-2020
Class II · Moderate risk Terminated

Atorvastatin Calcium Tablets

Reason Presence of foreign substance: Foreign matter has been identified as latex glove in one lot of Atorvastatin Calcium Tablets USP 40 mg.

Sun Pharmaceutical Industries, Inc. NDC 63304-829-05 D-1047-2020
Class II · Moderate risk Terminated

Sotalol HCL Tablets

Reason Presence of particulate matter. presence of metal particles.

Mylan Pharmaceuticals Inc. NDC 00378-5123-01 D-1031-2020
Class II · Moderate risk Terminated

Theophylline

Reason CGMP Deviations: poor manufacturing practices resulted in Labeling: Incorrect or Missing Lot and/or Exp Date, product incorrectly labeled with incorrect lot and expiration date.

Nostrum Laboratories Inc NDC 29033-001-01 D-1059-2020
Class II · Moderate risk Terminated

Acetaminophen 500 mg tablet packaged in a) 30-count bottles

Reason Presence of Foreign Tablets/Capsules: Complaint involving one Women's Prenatal dietary supplement tablet commingled in a bottle of Extra Strength Acetaminophen 500 mg contents 1000 count bottle

H J Harkins Company Inc dba Pharma Pac NDC 52959-0002-30 D-1005-2020
Class II · Moderate risk Terminated

Epinephrine Injection USP

Reason CGMP Deviations: Precautions taken due to Out-of-specification for trigger force for a non-marketed lot number that shares the same component.

Teva Pharmaceuticals USA NDC 0093-5986-27 D-1260-2020
Class II · Moderate risk Terminated

Sodium Chloride 0.9% Injection

Reason CGMP Deviation: Chemical indicators were not positioned properly during sterilization process.

Fresenius Medical Care Holdings, Inc. D-1064-2020
Class III · Low risk Terminated

PrediniSONE Tablets

Reason Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has been identified on Prednisone Tablets USP 5 mg

Par Pharmaceutical Inc. NDC 0603-5337-31 D-1035-2020
Class II · Moderate risk Terminated

Peppermint Lip Moisturizer

Reason Superpotent drug: This lot of SPF containing lip balm contains up to 150% of the label claim for active ingredient Oxybenzone.

Yusef Manufacturing Laboratories, LLC D-1251-2020
Class II · Moderate risk Terminated

Daytrana

Reason Defective Delivery System: Out of specification for mechanical peel and shear.

Noven Therapeutics, LLC NDC 68968-5555-3 D-1045-2020
Class II · Moderate risk Terminated

Daytrana

Reason Defective Delivery System: Out of specification for mechanical peel and shear.

Noven Therapeutics, LLC NDC 68968-5554-3 D-1044-2020
Class II · Moderate risk Terminated

Daytrana

Reason Defective Delivery System: Out of specification for mechanical peel and shear.

Noven Therapeutics, LLC NDC 68968-5553-3 D-1043-2020
Class II · Moderate risk Terminated

Daytrana

Reason Defective Delivery System: Out of specification for mechanical peel and shear.

Noven Therapeutics, LLC NDC 68968-5552-3 D-1042-2020