DrugNov 28, 2018
L. Perrigo Company Antacid Tablets, Calcium Carbonate chewable tablets, 750mg, 60-count recall — FDA D-0266-2019
Presence of foreign substance: Product found to contain metal particles.
Class IIFDA: TerminatedL. Perrigo Company
Recall history in this database
Classification mix: Class III: 3, Class II: 3.
DrugMay 23, 2018
Scopolamine Transdermal Therapeutic System, 1 mg/3 days, a) 4-count (NDC 45802-580-84) recall — FDA D-0816-2018
Defective delivery system
Class IIFDA: TerminatedL. Perrigo Company
DrugJul 5, 2017
L. Perrigo Company Walgreens Daytime and Nighttime Cold & Flu recall — FDA D-0925-2017
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…
Class IIIFDA: TerminatedL. Perrigo Company
DrugMar 8, 2017
L. Perrigo Company Salicylic Acid Cream, 6%, 400g bottle recall — FDA D-0504-2017
Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
Class IIIFDA: TerminatedL. Perrigo Company
DrugMar 8, 2017
L. Perrigo Company Salicylic Acid Shampoo, 6%, 177 mL bottle recall — FDA D-0503-2017
Failed Impurities/Degradation Specifications: The API for these products had an out of specification result for an organic impurity.
Class IIIFDA: TerminatedL. Perrigo Company
DrugJan 25, 2017
Clindamycin Phosphate and Benzoyl Peroxide Gel, 1.2%/5%, 45 g tubes recall — FDA D-0434-2017
Microbial Contamination of Non-Sterile Product; small number of tubes may include the presence of mold on the cap
Class IIFDA: TerminatedL. Perrigo Company
Understanding this recall history
This page summarizes recall records in which the official source identifies L. Perrigo Company as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.