FDA recall D-0346-2022

Perrigo Company PLC · Class II · drug

Product

Perrigo Fexofenadine Hydrochloride tablets, 12HR, 60mg Antihistamine, 100 count bottle, Made in the Czech Republic, Distributed by Perrigo Allergan, MI 49010 NDC 45802-425-78 UPC 3 45802 425 78 2

Reason for recall

Failed Impurities/Degradation Specifications; Out of specification result obtained for impurity A during stability testing.

Distribution

Nationwide in the USA

Key facts

Status
Terminated
Initiation date
2021-07-27
Report date
2022-01-12
Termination date
2022-11-08
Voluntary/Mandated
Voluntary: Firm initiated
Location
Allegan, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0346-2022