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FDA Drug Recalls

Every FDA drug enforcement recall Public Health Trace has on record, republished from openFDA's official drug enforcement database. See Health Alerts for current, active recalls alongside outbreaks and advisories.

Drug recall information is sourced from the FDA's structured openFDA Enforcement Reports. Newly announced recalls may appear on FDA.gov before they become available in the structured dataset. See Methodology for how Public Health Trace imports and refreshes this data.

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Showing 10,941–10,960 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Atorvastatin Calcium Tablets, 40 mg*, packaged in a) 90-count bottles (NDC 0378-3952-09) and b) 500-count bottles (NDC 0378-3952-07); Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.

by Mylan Pharmaceuticals Inc.

Reason
Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
Recall initiated
March 20, 2017
Reported by FDA
April 5, 2017
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass II

Atorvastatin Calcium Tablets, 20 mg*, packaged in a) 90-count bottles (NDC 0378-3951-09) and b) 500-count bottles (NDC 0378-3951-07); Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.

by Mylan Pharmaceuticals Inc.

Reason
Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
Recall initiated
March 20, 2017
Reported by FDA
April 5, 2017
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass II

Atorvastatin Calcium Tablets, 10 mg*, packaged in a) 90-count bottles (NDC 0378-3950-77); b) 90-count bottles (NDC 0378-3950-09); c) 500-count bottles (NDC 0378-3950-05); d) 500-count bottles (NDC 0378-3950-07), Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A.

by Mylan Pharmaceuticals Inc.

Reason
Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
Recall initiated
March 20, 2017
Reported by FDA
April 5, 2017
Distribution
Nationwide in the USA and Puerto Rico

View recall →

Drug Recall Terminated Historical recordClass II

Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a) 100 count (NDC 68382-033-01) and b) 500 count (NDC 68382-033-05) bottles, Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ

by Zydus Pharmaceuticals USA Inc

Reason
Failed Dissolution Specifications; 9 month long term stability
Recall initiated
March 15, 2017
Reported by FDA
April 5, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Levofloxacin Injection in 5% Dextrose, 750 mg in 150 mL 5% Dextrose, Rx only, Manufactured for: Claris Lifesciences Inc. North Brunswick NJ, 08902, By: Claris Injectable Ltd. Gujarat, India, NDC 36000-048-24

by Claris Lifesciences Inc

Reason
Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
Recall initiated
March 10, 2017
Reported by FDA
April 5, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Fluconazole Injection, USP, 400 mg in 200 mL, Rx only, Manufactured for: Claris Lifesciences Inc. North Brunswick NJ, 08902, By: Claris Injectable Ltd. Gujarat, India, NDC 36000-003-06

by Claris Lifesciences Inc

Reason
Lack of Assurance of Sterility: there is potential of a leak from the primary container which may result in a potential breach of sterility and contamination of the product.
Recall initiated
March 10, 2017
Reported by FDA
April 5, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Desonide Ointment, 0.05%, NET WT 60 grams tubes, Rx only, E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc., Melville, New York 11747, NDC 0168-0309-60

by Fougera Pharmaceuticals Inc.

Reason
Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may contain tubes of Desonide Ointment labeled as Ketoconazole Cream
Recall initiated
March 2, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Testosterone Cypionate Injection , USP, 200 mg/mL, 1 mL vial , For Intramuscular Use Only, Rx Only, Distributed by Sun Pharma Ind. Inc., NJ 08512, Manufactured by Sun Pharma Ind. Ltd. India, NDC 62756-015-40

by Sun Pharmaceutical Industries, Inc.

Reason
Presence of Particulate Matter
Recall initiated
March 15, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Famciclovir tablets, 500 mg, packaged in 30-count unit dose cartons, Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-307-13

by AVKARE Inc.

Reason
Failed impurities/ degradation specifications: Product was above specification for unknown impurities.
Recall initiated
February 15, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 900 mg/180 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-30).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Recall initiated
March 7, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide within US

View recall →

Drug Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 750 mg/150 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-205-25).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Recall initiated
March 7, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide within US

View recall →

Drug Recall Terminated Historical recordClass III

Quillivant XR (methylphenidate HCl) for extended-release oral suspension, 300 mg/60 mL (25mg/5mL), Rx Only, Distributed by: NextWave Pharmaceuticals, Inc. A subsidiary of Pfizer Inc, New York, NY 10017 Manufactured by: Tris Pharma, Inc., Monmouth Junction, NJ 08852 (NDC 24478-190-10).

by PFIZER INC

Reason
Failed Dissolution Specifications: Dissolution at 8 hour was out of specification at 12 month at 25 degree Celsius.
Recall initiated
March 7, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide within US

View recall →

Drug Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, 30-count bottle, Rx only, Distributed by: The Kroger Co., 1014 Vine Street, Cincinnati, OH 45202; Manufactured for: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534; Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045; NDC 68645-493-54.

by Legacy Pharmaceutical Packaging LLC

Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Recall initiated
March 7, 2017
Reported by FDA
March 29, 2017
Distribution
Product was shipped to distribution centers in TN, IN, and AZ then further shipped the product to retail pharmacies nationwide in the USA.

View recall →

Drug Recall Terminated Historical recordClass II

ATENOLOL Tablets, USP, 50 mg, packaged in a) 100-count bottles (NDC 68382-023-01) and b) 1000-count bottles (NDC 68382-023-10), Rx only, Manufactured by: Cadila Healthcare Ltd., India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534.

by Zydus Pharmaceuticals USA Inc

Reason
Presence of Foreign Tablets/Capsules: Customer complaint that a bottle of atenolol 50 mg Tablets USP contained a paroxetine 20 mg tablet.
Recall initiated
March 6, 2017
Reported by FDA
March 29, 2017
Distribution
Nationwide in the USA and Puerto Rico.

View recall →

Drug Recall Terminated Historical recordClass III

A+D Diaper Rash Cream with Dimethicone 1% and Zinc Oxide 10%, Packaged in a) 1.5 oz (42.5g) ( UPC 041100811288), b) 3 oz 85g (UPC 041100811301), c) 4 oz (113g) (UPC 041100811325), Distributed by: Bayer Healthcare LLC, Whippany, NJ 07981

by Bayer HealthCare Pharmaceuticals, Inc.

Reason
Labeling: Incorrect/Undeclared Excipients: Firm is recalling A+D Diaper Rash Cream due to a labeling claim issue.
Recall initiated
February 21, 2017
Reported by FDA
March 29, 2017
Distribution
US Nationwid, Puerto Rico, and Iceland

View recall →

Drug Recall Terminated Historical recordClass III

Buffered Lidocaine, 1%, In Sodium Bicarbonate 8.4%, 1 mL Total Volume in a 3 mL syringe, Local anesthetic use, Rx only, PharMEDium, Product code 2K2466

by PharMEDium Services, LLC

Reason
Labeling; Label Mixup; outer packaging is incorrectly labeled as Buffered Lidocaine 1% instead of correctly as Buffered Lidocaine 0.9%
Recall initiated
January 27, 2017
Reported by FDA
March 22, 2017
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

KOJIC ACID 8%/AZELAIC ACID 15% CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason
Lack of Assurance of Sterility: There are also CGMP Deviations.
Recall initiated
February 10, 2017
Reported by FDA
March 22, 2017
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

INTIMATE BLEACHING CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason
Lack of Assurance of Sterility: There are also CGMP Deviations.
Recall initiated
February 10, 2017
Reported by FDA
March 22, 2017
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

GENTLE SUPREME BLEACHING CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason
Lack of Assurance of Sterility: There are also CGMP Deviations.
Recall initiated
February 10, 2017
Reported by FDA
March 22, 2017
Distribution
Nationwide within the United States

View recall →

Drug Recall Terminated Historical recordClass II

CUSTOM LIGHTENING/BRIGHTENING CREAM, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

by Synergy Rx

Reason
Lack of Assurance of Sterility: There are also CGMP Deviations.
Recall initiated
February 10, 2017
Reported by FDA
March 22, 2017
Distribution
Nationwide within the United States

View recall →

Data last updated:

This information is republished from FDA's Recall Enterprise System through openFDA. Public Health Trace does not verify or supplement it, is not affiliated with the FDA, and does not provide medical advice -- always follow the guidance of your pharmacist, physician, or the recalling company for any medication you take. Read the full medical disclaimer.