FDA Drug recall D-1420-2015
Felodipine Extended-Release Tablets, 2.5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-368…
- FDA Drug
- Class III
- terminated
- Published 2015-09-16
On 2015-09-16 the FDA classified a Class III recall of Felodipine Extended-Release Tablets, 2.5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-368… by Mutual Pharmaceutical, citing chemical Contamination; benzophenone leached from the product label varnish.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1420-2015 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2015-07-16 |
| Published | 2015-09-16 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Mutual Pharmaceutical |
| Distribution | US |
Product
Felodipine Extended-Release Tablets, 2.5 mg, 100 count bottles, Rx only, Mutual Pharmaceutical Co. Inc., Philadelphia, PA --- NDC 53489-368-01
Reason
Chemical Contamination; benzophenone leached from the product label varnish
Identifiers
| code_info | lot #s: 6669101 & 6669201, exp 12/15 and 6708201 & 6708301, exp 8/16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1420-2015%22
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