Skip to content
Recall Observatory FDA recall evidence

Drug product

Pramipexole Dihydrochoride Tablets 0.25 mg, 90-count bottle, Rx Only, Manufactured by: Cadila Healthcare Ltd Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC 68382-197-16

D-1444-2019

May 06, 2019

Class II

Product summary

Firm
Zydus Pharmaceuticals USA Inc
Event
Event 82827
Status
Terminated
Classification
Class II
Quantity
215,760 90-count bottles
Official record key
drug-enforcement:D-1444-2019

Official wording

Reason: CGMP Deviations: Cross Contamination with other products due to CGMP cleaning failure.

Code information: Lots: M706802, M706804, M706907, M706909, M707028, EXP May-19; M714180, M714181, EXP Oct-19; M717063, M717064, M801705, M801706, M801707, M801708, M714923, M714924, M714925 EXP Dec-19; M808307, M808308, M808309, M808310, EXP May-20; M812479, M812481, M812482, M812483, EXP Jul-20; M815787 M815789, M815790, M815791, M815788, EXP Sep-20; M820266, M820267, M820268, M820269, M820265 EXP Nov-20; M903040, M903041, M903042 EXP Jan-21.

Distribution pattern: Nationwide in the USA

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviations