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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 4,281–4,300 of 17,937 drug recalls

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by Target Corporation, Minneapolis, MN 55403. NDC: 11673-759-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, MADE WITH PRIDE & CARE FOR H-E-B SAN ANTONIO, TX 78204. NDC: 37808-759-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by: Walmart, Inc., Bentonville, AR 72716. NDC: 49035-042-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by Target Corp., Minneapolis, MN 55403 NDC: 11673-130-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY DOLGENCORP, LLC, 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072. NDC: 55910-251-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY: Walmart Inc., Bentonville, AR 72716. NDC: 49035-959-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-818-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed By Perrigo, Allegan, MI 49010. NDC: 0113-8959-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, DISTRIBUTED BY THE KROGER CO. CINCINNATI, OHIO 45202. NDC: 30142-818-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Infant's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, Distributed by: CVS Pharmacy, Inc., One CVS Drive, Woonsocket, RI 02895. NDC: 59779-946-16

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, Distributed by Target Corporation, Minneapolis, MN 55403. NDC: 11673-133-16

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. NDC: 0363-0971-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Children's Cherry Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 45802-203-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 4 FL OZ (118 mL) per bottle, Distributed by: Rugby Laboratories, 17177 N Laurel Park Drive, Suite 233, Livonia, MI 48152. NDC: 0536-1321-97

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Children's Pain & Fever Bubblegum Flavored Acetaminophen Suspension (160mg/5ml), 4 fl oz (118 mL) per bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716. NDC: 49035-313-26

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass II

Acetaminophen Oral Suspension Grape Flavor, 160 mg per 5 mL, 16 fl oz (473 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 50941-009-43

by Perrigo Company PLC

Reason
CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Recall initiated
October 26, 2021
Reported by FDA
March 2, 2022
Distribution
Nationwide in the USA

View recall →

Drug Recall Terminated Historical recordClass III

Bortezomib, 3.5 mg/vial, Single-Dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-865-60

by Dr. Reddy's Laboratories, Inc.

Reason
Failed stability specifications
Recall initiated
January 19, 2022
Reported by FDA
March 2, 2022
Distribution
USA Nationwide

View recall →

Drug Recall Terminated Historical recordClass III

Azacitidine, 100mg/vial, One Single-dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-465-62

by Dr. Reddy's Laboratories, Inc.

Reason
Failed stability specifications
Recall initiated
January 19, 2022
Reported by FDA
March 2, 2022
Distribution
USA Nationwide

View recall →

Drug Recall Terminated Historical recordClass III

Azacitidine, 1,00mg/Vial, One Single-dose Vial, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Visakhapatnam - 530 046, India, NDC 43598-305-62

by Dr. Reddy's Laboratories, Inc.

Reason
Failed stability specifications
Recall initiated
January 19, 2022
Reported by FDA
March 2, 2022
Distribution
USA Nationwide

View recall →

Drug Recall Terminated Historical recordClass II

Lung Cleaner (saline eucalyptus) inhaler, 37 oz cans, Manufactured For: The Lung Cleaner LLC Boulder, CO 80302

by Pharmasol Corporation

Reason
cGMP deviations
Recall initiated
January 11, 2022
Reported by FDA
March 2, 2022
Distribution
Product was distributed to a client in Colorado.

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.