MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2019-07-12 for COBAS TAQSCREEN MPX TEST, V2.0 5969492190 manufactured by Roche Molecular Systems, Inc..
Report Number | 2243471-2019-00029 |
MDR Report Key | 8786165 |
Report Source | FOREIGN |
Date Received | 2019-07-12 |
Date of Report | 2019-10-23 |
Date of Event | 2019-06-23 |
Date Mfgr Received | 2019-06-24 |
Date Added to Maude | 2019-07-12 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | NA STACIE-ANN CREIGHTON |
Manufacturer Street | 1080 US HWY 202 S NA |
Manufacturer City | BRANCHBURG NJ 08876 |
Manufacturer Country | US |
Manufacturer Postal | 08876 |
Manufacturer Phone | 9082537112 |
Manufacturer G1 | NA |
Manufacturer Street | NA NA |
Manufacturer City | NA |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | COBAS TAQSCREEN MPX TEST, V2.0 |
Generic Name | ASSAY, HYB AND/OR NUCLEIC ACID AMP FOR DETECTION OF HCV RNA, HIV RNA |
Product Code | MZP |
Date Received | 2019-07-12 |
Model Number | NA |
Catalog Number | 5969492190 |
Lot Number | E18108 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ROCHE MOLECULAR SYSTEMS, INC. |
Manufacturer Address | 1080 US HIGHWAY 202 SOUTH NA BRANCHBURG NJ 08876 US 08876 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2019-07-12 |