L. Perrigo Company

Complete recall history across all FDA and CPSC categories — 21 total recalls

L. Perrigo Company appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Drug Recalls (21)

FDA drug safety enforcement actions by L. Perrigo Company

Date Product Reason Class
Feb 9, 2023 aller-ease, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons, Pac... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Allergy ALLER-FEX, Fexofenadine Hydrochloride Tablets, 180 mg, 180-count cart... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Non-Drowsy Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 150-co... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Allergy, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count ... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Picnic, Fexofenadine Hydrochloride Tablets, 180 mg, Antihistamine, 90-count c... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30-count cartons (... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 15-count cartons,... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Fexofenadine Hydrochloride Tablets, 180 mg, 100-count cartons, Distributed by... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, 30-count cartons,... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 allergyrelief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)30-c... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a) 30... Failed Impurities/Degradation Specifications Class II
Feb 9, 2023 allergy relief, Fexofenadine Hydrochloride Tablets, 180 mg, packaged in a)15-... Failed Impurities/Degradation Specifications Class II
Nov 6, 2018 Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count bottle, ... Presence of foreign substance: Product found to contain metal particles. Class II
May 11, 2018 Scopolamine Transdermal Therapeutic System, 1 mg/3 days, a) 4-count (NDC 4580... Defective delivery system Class II
Nov 8, 2017 Maximum Strength Zephrex-D, Pseudoephedrine HCl, 30 mg, Nasal Decongestant. ... Microbial Contamination of Non-Sterile Products Class II
Jun 5, 2017 Walgreens Daytime and Nighttime Cold & Flu, packaged in combo pack of two pla... Labeling: Label Mix-Up - This product is being recalled due to an incorrect p... Class III
Jun 1, 2017 Option 2, Levonorgestrel Tablet, 1.5 mg, Emergency Contraceptive, 1 Tablet pe... Defective Container: Carton is missing the tablet blister strip and tablet. Class II
Feb 13, 2017 Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Y... Failed Impurities/Degradation Specifications: The API for these products had ... Class III
Feb 13, 2017 Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruh... Failed Impurities/Degradation Specifications: The API for these products had ... Class III
Dec 28, 2016 Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes, Rx Only,... Microbial Contamination of Non-Sterile Product; small number of tubes may inc... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.

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