US Drug Recall Register
Class III · Low risk Terminated Initiated Jul 16, 2015 (11 years ago)

Felodipine Extended-Release Tablets, 5 mg, 100 count bottles, Rx only, Mutual…

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

Why it was recalled

Chemical Contamination; benzophenone leached from the product label varnish

What was recalled

Felodipine Extended-Release Tablets, 5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-369-01

Recalling firm
Mutual Pharmaceutical Company, Inc.
NDC code
53489-369-01
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1421-2015

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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