US Drug Recall Register
Class III · Low risk Terminated Initiated Oct 23, 2020 (6 years ago)

Felodipine Extended Release Tablets, USP 10 mg,100-count bottle, Rx only, Distributed by…

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

Why it was recalled

Failed impurities/ degradation specifications: Out of specification impurity results were observed during routine testing of stability samples for the impurity Felodipine Related compound A

What was recalled

Felodipine Extended Release Tablets, USP 10 mg,100-count bottle, Rx only, Distributed by: Heritage Pharmaceuticals Inc. East Brunswick, NJ 08816 Made in India, NDC 23155-050-01

Recalling firm
Heritage Pharmaceuticals Inc
NDC code
23155-050-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0108-2021

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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