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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 4,261–4,280 of 17,937 drug recalls

Drug Recall Terminated Historical recordClass II

Maximum Strength No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC, 410 TERRY AVENUE N. SEATTLE, WA 9810. NDC 72288-388-10

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

Maximum Strength No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC, 410 TERRY AVENUE N. SEATTLE, WA 9810. NDC 72288-388-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY TOPCO ASSOCIATES LLC., ELK GROVE VILLAGE, IL 60007. NDC 36800-907-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Dist. by Target Corp., Mpls., MN 55403. NDC 11673-935-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, Distributed by SUPERVALU INC., Eden Prairie, MN 55344 USA. NDC 41163-343-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: BETTER LIVING BRANDS LLC, P.O. BOX 99, PLEASANTON, CA 94566-0009. NDC 21130-813-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: RITE AID, 30 HUNTER LANE, CAMP HILL, PA 17011. NDC 11822-6378-1

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY FOODHOLD U.S.A., LLC, LANDOVER, MD 20785. NDC 41520-108-10

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

Severe Congestion No Drip Nasal Spray Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY DOLGENCORP, LLC, 100 MISSION RIDGE, GOODLETTSVILLE, TN 37072. NDC 55910-511-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05%, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY FOODHOLD U.S.A., LLC, LANDOVER, MD 20785. NDC 41520-108-10

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

Severe Congestion Nasal Spray, No Drip Plus Menthol, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, Packaged by Perrigo Company for: Big Lots Stores, Inc., P.O. Box 28523, Columbus, OH 43228-0523. NDC: 50594-719-10

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

Maximum Strength Plus Menthol No Drip Nasal Spray, Oxymetazoline HCl 0.05% Nasal Decongestant, 1 FL Oz (30 mL) per bottle, DISTRIBUTED BY: AMAZON.COM SERVICES LLC 410 TERRY AVENUE N.SEATTLE, WA 98109. NDC: 72288-703-10

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 Bubble Gum Flavored Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 0113-0020-26

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 Bubble Gum Flavored Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 11673-105-26

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 Pain & Fever Acetaminophen, 160 mg per 5 mL Oral Suspension combo pack. DS SR APAP 160MG CHLD BBGM/DF CHRY/GRP. UPC: 3 70030 11637 9

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 Bubble Gum Flavored Oral Suspension (160 mg/5 ml), two 4 FL OZ (118 mL) bottles per pack, Distributed by Walmart 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

Infant's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY: Wal-Mart Stores, Inc., Bentonville, AR 72716. NDC: 49035-946-16

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: Wal-Mart Stores, Inc., Bentoneville, AR 72716. NDC: 49035-766-16

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 THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-766-16

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 THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-766-16

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 →

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.