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

Propafenone Hydrochloride tablets, 150 mg, packaged in 10 x 10 unit dose cards (100-count…

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.

Other Chloride recalls

See all