Perrigo Company PLC: Drug Recall

Recall #D-0596-2022 · 10/26/2021

Class II: Risk

Recall Details

Recall Number: D-0596-2022
Classification: Class II
Product Type: Drug
Recalling Firm: Perrigo Company PLC
Status: Terminated
Date Initiated: 10/26/2021
Location: Allegan, MI, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 5,184 bottles

Reason for Recall

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

Product Description

Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202. NDC: 30142-766-16

Distribution Pattern

Nationwide in the USA

Other Recalls by Perrigo Company PLC

Class II: Risk 10/26/2021

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II: Risk 10/26/2021

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II: Risk 10/26/2021

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II: Risk 10/26/2021

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.
Class II: Risk 10/26/2021

CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.

View all recalls by Perrigo Company PLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.