MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer,foreign report with the FDA on 2020-01-15 for COREGA TABS manufactured by Block Drug Co., Inc..
Report Number | 1020379-2020-00004 |
MDR Report Key | 9590550 |
Report Source | CONSUMER,FOREIGN |
Date Received | 2020-01-15 |
Date of Report | 2020-01-06 |
Date Mfgr Received | 2020-01-06 |
Date Added to Maude | 2020-01-15 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Street | PO BOX 13398 RESEARCH TRIANGLE PARK |
Manufacturer City | NC 27709 |
Manufacturer Country | US |
Manufacturer Postal | 27709 |
Manufacturer Phone | 8888255249 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | COREGA TABS |
Generic Name | DENTURE CLEANSER |
Product Code | EFT |
Date Received | 2020-01-15 |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BLOCK DRUG CO., INC. |
Manufacturer Address | MEMPHIS, TN US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-01-15 |