RecallDepth
Class II Terminated

Amlodipine and Benazapril HCL Capsules, USP, 5 mg/10 mg, 100 count bottles, Mylan Pharmaceuticals, Inc., Morgantown, WV --- NDC 0378-6896-01

Company
Mylan Pharmaceuticals Inc.
Recall Initiated
April 24, 2018
Posted
May 23, 2018
Recall Number
D-0819-2018
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
25,488 bottles
Firm Location
Morgantown, WV, United States

Reason for Recall

cGMP Deviations; cleaning process for equipment used to manufacture the specified batches was not followed according to procedure

Distribution

Product was distributed throughout United States

Lot / Code Info

Lot Numbers# 3083005, 3083006, 3086121, and 3086122, exp Jan 2019

More recalls by Mylan Pharmaceuticals Inc.

View all recalls by this company →

Other recent Class II Drug recalls