MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-31 for HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP 1103 manufactured by Heartware, Inc..
Report Number | 3007042319-2020-02767 |
MDR Report Key | 9903582 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2018-09-18 |
Date Mfgr Received | 2020-03-12 |
Device Manufacturer Date | 2018-07-02 |
Date Added to Maude | 2020-03-31 |
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 ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635055378 |
Manufacturer G1 | HEARTWARE, INC. |
Manufacturer Street | 14400 NW 60TH AVE |
Manufacturer City | MIAMI LAKES FL 33014 |
Manufacturer Country | US |
Manufacturer Postal Code | 33014 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HEARTWARE VENTRICULAR ASSIST SYSTEM - PUMP |
Generic Name | VENTRICULAR (ASSIST) BYPASS |
Product Code | DSQ |
Date Received | 2020-03-31 |
Model Number | 1103 |
Catalog Number | 1103 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HEARTWARE, INC. |
Manufacturer Address | 14400 NW 60TH AVE MIAMI LAKES FL 33014 US 33014 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Required No Informationntervention | 2020-03-31 |