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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 12,581–12,600 of 17,974 drug recalls

Drug Recall Terminated Historical recordClass II

Pedi MVI a) 5 mL, b) 10 mL syringe, Rx Only, Compounded by Option Care 148, San Antonio, TX 78232-5045

by Walgreens Infusion Services

Reason
Lack of Assurance of Sterility
Recall initiated
November 10, 2015
Reported by FDA
January 6, 2016
Distribution
Texas

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Drug Recall Terminated Historical recordClass III

Cetirizine HCl 10 mg Tablet, 14 count blister packs, sold over the counter under the following brands, GoodSense brand distributed by Perrigo, Allegan, MI; Equaline brand distributed by; Supervalu Inc, Eden Prairie, MN (NDC 41163-458-66); Good Neighbor Pharmacy brand, distributed by AmerisourceBergen, Chesterbrook, PA (NDC 24385-998-74); HEB brand, San Antonio, TX (NDC 37808-458-66); Rexall brand Packaged for Dolgencorp LLC, Goodlettsville, TN (NDC 55910-699-66 UPC: 370030659432), HyVee brand, distributed by Hy-Vee Inc., West Des Mones, IA (NDC 42507-458-66); Smart Sense brand distributed by Kmart Corporation, Hoffman Estates, IL (NDC 49738-458-66); Kroger brand distributed by The Kroger Co, Cincinnati, OH (NDC 30142-458-66); Leader brand distributed by Cardinal Health, Dublin, OH (NDC 49781-106-14; CVS Pharmacy brand distributed by CVS Pharmacy, Inc., Woonsocket, RI (NDC 59779-458-66); Healthy Accents brand distributed by DZA Brands, LLC, Salisbury, NC (NDC 55316-458-66); Safeway Care brand distributed by Safeway Inc., Pleasanton, CA (NDC 21130-458-66); Topcare brand distributed by Topsco Associates, LLC, Skokie, IL (NDC 36800-458-66); Wal-Zyr brand distributed by Walgreens Co, Deerfield, IL (NDC 0363-0495-66); Being Well brand distributed by Save-A-Lot Food Stores, Ltd, Earth City, MO (NDC 46994-458-66); CareOne brand distributed by FoodHold, USA LLC, Landover, MD (NDC 41520-458-66); Shoprite brand distributed by Wakefern Food, Corp, Keasbey, NJ (NDC 41190-458-66 UPC: 041190223343); Shopko brand distributed by Shopko Stores Operating Co., LLC, Green Bay, WI (NDC 37012-458-66 UPC: 370030677689); Western Family brand distributed by Western Family Foods, Inc., Portland, OR (NDC 55312-458-66 UPC: 015400121026)

by Perrigo Company PLC

Reason
Failed Impurity/Degradations Specifications; impurity identified as cetirizine monosaccharide ester
Recall initiated
September 28, 2015
Reported by FDA
December 30, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass III

HPMC Visoelastic, 8,000 cps, Reference 51082, LT5108 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741

by Oasis Medical, Inc.

Reason
Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Recall initiated
October 19, 2015
Reported by FDA
December 30, 2015
Distribution
Nationwide and Saudi Arabia, Israel, Chile, Norway, Ecuador, Greece, Switzerland, Canada, England, Columbia, Poland, South Africa, Germany, Pakistan, El Salvador, Dubai, Belgium

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Drug Recall Terminated Historical recordClass III

HPMC Visoelastic Topical, 8,000 cps, Reference 5200, 1.5 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741

by Oasis Medical, Inc.

Reason
Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Recall initiated
October 19, 2015
Reported by FDA
December 30, 2015
Distribution
Nationwide and Saudi Arabia, Israel, Chile, Norway, Ecuador, Greece, Switzerland, Canada, England, Columbia, Poland, South Africa, Germany, Pakistan, El Salvador, Dubai, Belgium

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Drug Recall Terminated Historical recordClass III

HPMC Visoelastic, 20,000 cps, Reference 5122, 515 (Private Label), 600102-001 (Private Label), 600103-001 (Private Label), 2.0 mL in 3-mL Syringe, OASIS Medical Inc, 514 South Vermont Avenue Glendora, CA 91741

by Oasis Medical, Inc.

Reason
Failed pH Specification: It has been determined that the pH of the lots recalled, may not meet specification at expiry.
Recall initiated
October 19, 2015
Reported by FDA
December 30, 2015
Distribution
Nationwide and Saudi Arabia, Israel, Chile, Norway, Ecuador, Greece, Switzerland, Canada, England, Columbia, Poland, South Africa, Germany, Pakistan, El Salvador, Dubai, Belgium

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Drug Recall Terminated Historical recordClass III

Irbesartan and Hydrochlorothiazide tablets USP 150 mg/ 12.5 mg, 90-count bottles, Rx only, Manufactured in Israel by: TEVA PHARMACEUTICAL INDUSTRIES LTD Jerusalem, 971010 Israel, Manufactured for: TEVA PHARMACEUTICAL INDUSTRIES USA Sellersville, PA 18960. NDC 0093-8238-98

by Teva Pharmaceutical Industries

Reason
Labeling: Incorrect or Missing Lot AND/OR Exp Date.
Recall initiated
October 20, 2015
Reported by FDA
December 23, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass III

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-count bottles (NDC 0025-2742-51), Rx only, Distributed by G.D. Searle LLC, Division of Pfizer Inc, NY, NY 10017.

by Pfizer Inc.

Reason
Failed Dissolution Specification
Recall initiated
December 2, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Ventolin HFA (albuterol sulfate) Inhalation Aerosol, 90 mcg per actuation, 200 Metered Inhalations, Rx Only, For Oral Inhalation Only, Net Wt. 18 g, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20

by GlaxoSmithKline, LLC

Reason
Defective Delivery System: Some canisters may not contain sufficient propellant to deliver the labeled claim of 200 actuations through the end of shelf life.
Recall initiated
December 3, 2015
Reported by FDA
December 16, 2015
Distribution
MS and VT

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Drug Recall Terminated Historical recordClass II

Kindest Kare Antimicrobial Foaming Handwash, Hand Soap, 0.75% Triclosan, 444 ml (15 fl oz) bottles, STERIS Corporation, 7501 Page Avenue, St. Louis, MO 63133, Reorder # 1452-RF, NDC 0519-1452-13, UPC (01)00724995 086251.

by Steris Corp

Reason
Labeling: Not Elsewhere Classified; Incorrect/Undeclared Excipients: Outdated previous version of label applied to products that incorrectly states one inactive ingredient.
Recall initiated
October 27, 2015
Reported by FDA
December 16, 2015
Distribution
Medical Center/Hospitals in FL, MO, and TN.

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Drug Recall Terminated Historical recordClass II

Rocuronium Bromide 50 MG/5ML INJ., Qty: 5 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0222-57

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Novolin 70/30, 100 Units/mL Solu., Qty: 1 Vial, MFG by: Novo Nordisk, A/S, Bagsvaerd, Denmark DK-2880, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0414-01

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Lorazepam 2 mg/mL Inj., Qty: 1 mL Vial, MFG by: West-Ward Pharma, Eatontown, NJ 07724, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0316-01

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Ascorbic Acid 500 MG/ML Inj., Qty: 50 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0431-16

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Vitamin B-Complex 100, Multi MG Inj, Qty: 30 mL Vial, MFG by: Mylan Institutional, Rockford, IL 61103, Repackaged by: RemedyRepack Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 52125-0873-02

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

Bicillin L-A 600000 Units/mL Inj., Qty: 20 mL Syringe, MFG by: King Pharma Inc., Bristol, TN 37620, Repackaged by: RemedyRepack, Inc., 625 Kolter Dr., Indiana, PA 15701, NDC 61786-0253-03

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Humulin 70/30, 100 Units/mL Inj, Qty: 10 mL Vial, MFG by: Lilly USA, LLC, Indianapolis, IN 46285, Repackaged by: Remedy Repack, Inc, 625 Kolter Dr, Indiana, PA 15701, NDC 52125-0415-08

by RemedyRePack Inc.

Reason
Labeling: Incorrect Instructions; RemedyRepack, Inc. a relabeler, is recalling these products due to incorrect storage instructions.
Recall initiated
November 11, 2015
Reported by FDA
December 16, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass III

MECLIZINE HYDROCHLORIDE TABLETS, 25 mg, Packaged in a) 100 ct Bottles (NDC: 60429-205-01) and b) 1000 ct Bottles (NDC: 60429-205-10), Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012.

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Recall initiated
November 25, 2015
Reported by FDA
December 16, 2015
Distribution
U.S. Nationwide

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Drug Recall Terminated Historical recordClass III

MECLIZINE HYDROCHLORIDE TABLETS, 12.5 mg, Packaged in 1000 ct Bottles, Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012. NDC: 60429-204-10.

by Golden State Medical Supply Inc.

Reason
Failed Impurities/Degradation Specifications: Out of specification for impurities.
Recall initiated
November 25, 2015
Reported by FDA
December 16, 2015
Distribution
U.S. Nationwide

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Drug Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIC (HCG) Sublingual Drops, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason
Penicillin Cross Contamination: potentially contaminated with penicillin
Recall initiated
June 8, 2015
Reported by FDA
December 9, 2015
Distribution
Nationwide

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Drug Recall Terminated Historical recordClass II

HUMAN CHORIONIC GONADOTROPIC (HCG) Injection, Rx, compounded by Life Science Pharmacy Inc., Harriman, NY

by Life Science Pharmacy Inc

Reason
Penicillin Cross Contamination: potentially contaminated with penicillin
Recall initiated
June 8, 2015
Reported by FDA
December 9, 2015
Distribution
Nationwide

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.