US Drug Recall Register
Class II · Moderate risk Terminated Initiated May 6, 2019 (7 years ago)

Pramipexole Dihydrochloride Tablets 0.5 mg, 90-count bottle, Rx only, Manufactured by…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

What was recalled

Pramipexole Dihydrochloride Tablets 0.5 mg, 90-count bottle, Rx only, Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08534. NDC 68382-198-16

Recalling firm
Zydus Pharmaceuticals USA Inc
NDC code
68382-198-16
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1446-2019

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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