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 2020-03-11 for OPEN PIVOT MECHANICAL HEART VALVE 500DM29 manufactured by Medtronic, Inc..
[182986998]
Product analysis: no product was returned. Conclusion: without the return of the product, no definitive conclusion can be made regarding the clinical observation. If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[182986999]
Medtronic received information that 1 year and 7 days post implant of this 29mm mitral mechanical valve, it was explanted and replaced with a non-medtronic device. The reason for the replacement was not reported. No additional adverse patient effects were reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3008592544-2020-00017 |
MDR Report Key | 9819428 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-11 |
Date of Report | 2020-04-02 |
Date of Event | 2020-02-21 |
Date Mfgr Received | 2020-03-23 |
Device Manufacturer Date | 2017-09-11 |
Date Added to Maude | 2020-03-11 |
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 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, INC. |
Manufacturer Street | 3800 ANNAPOLIS LANE |
Manufacturer City | MINNEAPOLIS MN 55447 |
Manufacturer Country | US |
Manufacturer Postal Code | 55447 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OPEN PIVOT MECHANICAL HEART VALVE |
Generic Name | HEART-VALVE, MECHANICAL |
Product Code | LWQ |
Date Received | 2020-03-11 |
Model Number | 500DM29 |
Catalog Number | 500DM29 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC, INC. |
Manufacturer Address | 3800 ANNAPOLIS LANE MINNEAPOLIS MN 55447 US 55447 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-11 |