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Perrigo Company Recalls
106 recalls on record · December 30, 2015 to March 2, 2022 · Drugs, Food & Beverage
Recalls by year
15
16
19
20
22
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
Also filed under
The recall feeds record what looks like the same company under more than one name:
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 30 count bottle,
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 24 count bottle, Made in the Czec
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Perrigo Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle, Made in the Czech Republic, Di
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Perrigo Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, 100 count bottle, Made in the Czech Republic, D
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls allergyrelief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, NDC 56062
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Meijer allergy relief, Fexofenadine Hydrochloride tablets, 24HR, 1800mg Antihistamine, packaged as a) 15 count bottle, N
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls MAJOR, Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle, Distributed by Major Pharmaceut
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Kroger Allergy Relief, Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 12 count bottle, Distributed by t
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg/Antihistamine packaged as a) 15 count bottle,
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 12HR, 60mg/Antihistamine 12 count bottle, Made with Pride
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Health Mart, Fexofenadine Hydrochloride tablets, 24HR, 180mg . Antihistamine 70 count bottle, Distributed by: Mckess
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls Health Mart, Fexofenadine Hydrochloride tablets, 12HR, 60mg . Antihistamine 12 count bottle, Distributed by: Mckesso
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls DG/health Aller.Ease, Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24HR, 10 count bottle, Distributed by:
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 60 mg Antihistamine, 12HR, packaged as a) 12 count bottle, NDC
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls CAREONE Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, packaged as a)30 count bottle,
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls berkley jensen, ALLERGY RELIEF, Fexofenadine Hydrochloride Tablets, 180 mg Antihistamine, 24HR, 150 count bottle, Made
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls basic+care, allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls basic+care, allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 150 count bottle, Made in the Czec
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls amazon, Allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 30 count bottle, Made in the Czech Re
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls GoodSense Aller.Ease, Fexofenadine hydrochloride 12 HR, 60 mg tablets, 24 count bottle, UPC 3 0113 0425 62 7; Made in t
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
January 12, 2022DrugsFDA
Perrigo Company PLC recalls EQUALINE aller-ease fexofenadine hydrochloride tablets, 180 mg, 24 HR, packaged as a) 15 count bottle, NDC 41163-571-22,
Hazard: Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.
September 30, 2020DrugsFDA
Perrigo Company PLC recalls Albuterol Sulfate Inhalation Aerosol, 90 mcg per actuation, 200 metered inhalations, Manufactured by: Catalent Pharma So
Hazard: Defective Delivery System: Sustained trend of failure to dispense complaints.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 200 tablets per bottle. [Brand, NDC] NDC Basic Care: 011
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic C
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 95 tablets per bottle. [Brand, NDC] NDC Basic Care: 0113-
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate:
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 90 tablets per bottle. [Brand, NDC] NDC Equate: 49035-608
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Cool Mint Ranitidine tablets, USP 150 mg, 65 tablets per bottle. [Brand, NDC] NDC Basic C
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 65 tablets per bottle. [Brand, NDC] NDC Care One: 41520-3
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.
March 25, 2020DrugsFDA
Perrigo Company PLC recalls Maximum Strength Acid Reducer, Ranitidine tablets, USP 150 mg, 50 tablets per bottle. [Brand, NDC] NDC DG Health: 55910-
Hazard: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.