L. Perrigo Recalls
28 recalls on record · January 23, 2013 to July 19, 2023 · Drugs
Recalls by year
13
17
18
23
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 19, 2023DrugsFDA
L. Perrigo Company recalls Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 36800-691-39), b)45-cou
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine, 90-count cartons, Distributed by: Thirty Madison, Inc
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 11673-617-22), b)30-coun
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls allergyrelief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)30-count cartons (NDC 56062-847-39); and b) 45-
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 0113-0847-39), and b) 45-count cartons
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Fexofenadine Hydrochloride Tablets, 180 mg, 100-count cartons, Distributed by: Perrigo, Allegan, MI 49010. NDC 45802-847
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-count cartons (NDC 79481-0847-0), b)30-coun
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Allergy ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg, 180-count cartons, Packaged by: Perrigo, 515 Eastern Ave.
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls aller-ease, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Packaged For: Your Military Exchanges, By: Per
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Distributed By: CVS Pharmacy, Inc., One CV
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 15-count cartons, Distributed By: Adusa Distribution, LLC, S
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Non-Drowsy Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 150-count cartons, Distributed By: BJ's Wholesale
Hazard: Failed Impurities/Degradation Specifications
July 19, 2023DrugsFDA
L. Perrigo Company recalls Allergy, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (NDC 72288-847-39), and b)150-count
Hazard: Failed Impurities/Degradation Specifications
November 28, 2018DrugsFDA
L. Perrigo Company recalls Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, OTC, [Healthy Accents brand NDC: 55316-014-
Hazard: Presence of foreign substance: Product found to contain metal particles.
May 23, 2018DrugsFDA
L. Perrigo Company recalls Scopolamine Transdermal Therapeutic System, 1 mg/3 days, a) 4-count (NDC 45802-580-84); b) 10-count (NDC 45802-580-46);
Hazard: Defective delivery system
December 27, 2017DrugsFDA
L. Perrigo Company recalls Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant. 24 softgel tablets per paper carton, Distri
Hazard: Microbial Contamination of Non-Sterile Products
July 5, 2017DrugsFDA
L. Perrigo Company recalls Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two plastic 12FL OZ (355 mL) bottles connected by
Hazard: Labeling: Label Mix-Up - This product is being recalled due to an incorrect product sleeve on the product twin pack. The incorrect product sleeve is for Day-Night Cold and Flu whereas the batch contains Day-Night Cough Liquid.
June 14, 2017DrugsFDA
L. Perrigo Company recalls Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet per box, Distributed By Perrigo, Allegan, MI
Hazard: Defective Container: Carton is missing the tablet blister strip and tablet.
March 8, 2017DrugsFDA
L. Perrigo Company recalls Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Al
Hazard: Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
March 8, 2017DrugsFDA
L. Perrigo Company recalls Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Alle
Hazard: Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
January 25, 2017DrugsFDA
L. Perrigo Company recalls Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only, Manufactured by Perrigo, Yeruham, Israel,
Hazard: Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
November 27, 2013DrugsFDA
L. Perrigo Co. recalls Acetaminophen suspension liquid, 160 mg/5 mL, grape flavor, 2 FL OZ (59 mL) bottle co-packaged with an oral dosing syrin
Hazard: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
November 27, 2013DrugsFDA
L. Perrigo Co. recalls Acetaminophen suspension liquid, 160 mg/5 mL, dye-free grape flavor, 2 FL OZ (59 mL) bottle co-packaged with an oral dos
Hazard: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
November 27, 2013DrugsFDA
L. Perrigo Co. recalls Acetaminophen suspension liquid, 160 mg/5 mL, cherry flavor, 2 FL OZ (59 mL) bottle co-packaged with an oral dosing syri
Hazard: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
November 27, 2013DrugsFDA
L. Perrigo Co. recalls Acetaminophen suspension liquid, 160 mg/5 mL, dye-free cherry flavor, co-packaged with an oral dosing syringe in a carto
Hazard: Defective Delivery System: There is a remote potential that cartons of product could be co-packaged with an oral dosing syringe without dose markings.
May 15, 2013DrugsFDA
L. Perrigo Co. recalls Liothyronine Sodium Tablets, USP, 5 mcg Rx ONLY, 100 count bottle, Distributed by: Paddock Laboratories, Inc., Minneap
Hazard: Failed Impurities/Degradation Specifications: 3 month stability testing.
April 3, 2013DrugsFDA
L. Perrigo Co. recalls PE Daytime Cold/Flu LiqGel, Multi Symptom Relief, Acetaminophen/Dextromethorphan HBr/Phenylephrine HCL 325/10/5 mg gel c
Hazard: Subpotent; 12 month time point for the active ingredient Phenylephrine HCl.
January 23, 2013DrugsFDA
L. Perrigo Co. recalls Prednisone tablets, USP, 10mg, Rx Only, Units of Use, NDC: a) 45802-303-67, 48-count Cartons, b) 45802-303-21, 21-count
Hazard: Presence of Foreign Substance(s); Perrigo has been notified of a recall by the manufacturer of this product, West-Ward Pharmaceuticals. This is a sub-recall due to tablets contaminated with trace amounts of food-grade lubricant, as well as stainless steel inclusions