US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 22, 2018 (8 years ago)

Catapres .2 (clonidine hydrochloride, USP) 0.2mg, 100-count bottles, Rx only, Dist. by…

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

Why it was recalled

Failed Dissolution Specifications: OOS resultsduring routine stability testing

What was recalled

Catapres .2 (clonidine hydrochloride, USP) 0.2mg, 100-count bottles, Rx only, Dist. by: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877 USA. Made in Germany. NDC 0597-0007-01

Recalling firm
Boehringer Ingelheim Pharmaceuticals, Inc.
NDC code
0597-0007-01
Origin
CT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0128-2019

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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