Product Safety Recalls

Product Recall Tracker

Recall D-0559-2023

Description: Glimepiride USP, 4 mg, 90 count-bottles, Rx only, Intas Pharm. Limited Pkg By: PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127, NDC 43063-0587-90

Recall D-0559-2023 Information

Mandated?Voluntary: Firm initiated
Recall NumberD-0559-2023
Event ID92081
DistributionNationwide in the US.
Quantity186 bottles
Recall ReasonCGMP deviations.
Drug ClassificationClass II
Drug Code Info20230510
Recall Initiation Date20230406
Report Date20230510
Classification Date20230501
Address727 N Ann Arbor Ave
Oklahoma City, OK 73127-5822
United States
Recalling FirmPD-Rx Pharmaceuticals, Inc.
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied. is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.