US Drug Recall Register
Class III · Low risk Terminated Initiated Aug 28, 2017 (9 years ago)

Propafenone Hydrochloride tablets

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed moisture limits: Out of specification for moisture content.

What was recalled

Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count box), Rx only, Manufactured By: Watson Pharmaceuticals 311 Bonnie Circle Corona, CA 92880, NDC 63739-509-10

Recalling firm
Mckesson Packaging Services
NDC code
63739-509-10
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1128-2017

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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