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Perrigo Company PLC

Recalls

Recalls by year

A bar chart of the number of recalls naming this company by year.

Recalls by year
YearRecalls
20191
202018
202281
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FDA Recall Terminated Historical recordClass II

DG/health Aller.Ease, Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24HR, 10 count bottle, Distributed by: Made in Czech Republic. Distributed by Dolgencorp, LLC, 100 Mission Ridge Goodlettsville, TN 37072. UPC 3 70030 65779 7

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 60 mg Antihistamine, 12HR, packaged as a) 12 count bottle, NDC 59779-425-53, UPC 0 50428 25414 1; b)24 count bottle, NDC 59779-425-62, UPC 0 50428 53435 9; Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, Made in Czech Republic

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

CAREONE Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, packaged as a)30 count bottle, NDC 41520-229-39, UPC 3 41520 31984 6; b)45 count bottle, NDC 41520-229-95 UPC 3 41520 31983 9; Made in the Czech Republic, Distributed by: Foodhold U.S.A. LLC Landover, MD 20785. Made in Czech Republic

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

berkley jensen, ALLERGY RELIEF, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 150 count bottle, Made in the Czech Republic, Distributed by: BJ's WHolesale Club 25 Research Drive Westborough, MA 01581

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

basic+care, allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech Republic, Distributed by: Perrigo Allergan, MI 49010, NDC 0113-7425-78 UPC 3 70030 14536 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

basic+care, allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 150 count bottle, Made in the Czech Republic, Distributed by: Perrigo Allergan, MI 49010, NDC 0113-7571-47 UPC 3 70030 11470 2

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

amazon, Allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 30 count bottle, Made in the Czech Republic, Distributed by: Amazon.com Services LLC 410 Terry Avenue N. Seattle, WA 98109 UPC 3 70030 11466 5

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

GoodSense Aller.Ease, Fexofenadine hydrochloride 12 HR, 60 mg tablets, 24 count bottle, UPC 3 0113 0425 62 7; Made in the Czech Republic, Distributed by: Perrigo Allergan MI 49010.

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22, UPC 0 41163 48067 4; b) 70 tablets per bottle, NDC 41163-571-01, UPC 0 41163 49847 1; Made in the Czech Republic, Distributed by: UNFI Providence, RI 02908.

by Perrigo Company PLC

Reason
Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
Published
January 12, 2022
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma Solutions, 160 N Pharma Drive, Morrisville, NC 27560, Distributed by: Perrigo, Allegan, MI 49010 NDC 45802-088-01

by Perrigo Company PLC

Reason
Defective Delivery System: Sustained trend of failure to dispense complaints.
Published
September 30, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-7852-01; NDC Berkley Jensen: 68391-852-56; NDC: CVS Health: 59779-540-01; NDC DG Health: 55910-011-01; NDC Kirkland: 63981-852-56; NDC Kroger: 30142-600-56; NDC Meijer: 41250-852-01; NDC Rite Aid: 11822-0852-4; NDC Walgreens: 0363-0852-01

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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FDA Recall Terminated Historical recordClass II

Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate: 49035-800-75; NDC Up & Up: 11673-950-75

by Perrigo Company PLC

Reason
CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
Published
March 25, 2020
Distribution
Nationwide

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This page lists recalls that name Perrigo Company PLC as the recalling firm in the official source notice. It is not a safety rating, ranking, or statement that the company acted negligently. Read the full medical disclaimer.