MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-11-14 for MEDTRONIC VENOUS RESERVOIR - 1600ML MVR1600 manufactured by Medtronic Mexico.
Report Number | 9612164-2019-04742 |
MDR Report Key | 9320257 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2019-11-14 |
Date of Report | 2019-11-14 |
Date of Event | 2019-10-15 |
Date Mfgr Received | 2019-10-15 |
Date Added to Maude | 2019-11-14 |
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 | PAULA BIXBY |
Manufacturer Street | 8200 CORAL SEA STREET NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635055378 |
Manufacturer G1 | MEDTRONIC MEXICO |
Manufacturer Street | AV. PASEO DEL CUCAPAH #10510 |
Manufacturer City | TIJUANA,BC 22570 |
Manufacturer Country | MX |
Manufacturer Postal Code | 22570 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MEDTRONIC VENOUS RESERVOIR - 1600ML |
Generic Name | RESERVOIR, BLOOD, CARDIOPULMONARY BYPASS |
Product Code | DTN |
Date Received | 2019-11-14 |
Returned To Mfg | 2019-11-08 |
Model Number | MVR1600 |
Catalog Number | MVR1600 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC MEXICO |
Manufacturer Address | AV. PASEO DEL CUCAPAH #10510 TIJUANA,BC 22570 MX 22570 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-11-14 |