PlainRecalls
FDA Drug Low Class III Terminated

Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01

Reported: September 16, 2015 Initiated: July 16, 2015 #D-1422-2015

Product Description

Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01

Reason for Recall

Chemical Contamination; benzophenone leached from the product label varnish

Details

Units Affected
63,975 bottles
Distribution
Nationwide
Location
Philadelphia, PA

Frequently Asked Questions

What product was recalled?
Felodipine Extended-Release Tablets, 10 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co Inc., Philadelphia, PA --- NDC 53489-370-01. Recalled by Mutual Pharmaceutical Company, Inc.. Units affected: 63,975 bottles.
Why was this product recalled?
Chemical Contamination; benzophenone leached from the product label varnish
Which agency issued this recall?
This recall was issued by the FDA Drug on September 16, 2015. Severity: Low. Recall number: D-1422-2015.