MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06,07 report with the FDA on 2003-02-20 for CARMEDA PEDIATRIC BIO-PROBE CBDP-38P 95140 manufactured by Medtronic Perfusion Systems.
[19901545]
Pt placed on ecmo in intensive care following surgery. After an unknown length of time, a leak began at the flow-probe. Before the unit could be changed out, the port broke completely. Pt died the following day.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2184009-2003-00009 |
MDR Report Key | 444427 |
Report Source | 01,05,06,07 |
Date Received | 2003-02-20 |
Date of Report | 2003-01-23 |
Date of Event | 2003-01-21 |
Date Mfgr Received | 2003-01-23 |
Date Added to Maude | 2003-02-26 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 0 |
Manufacturer Contact | LISA WEIK |
Manufacturer Street | 8299 CENTRAL AVENUE, NE |
Manufacturer City | MINNEAPOLIS MN 55432 |
Manufacturer Country | US |
Manufacturer Postal | 55432 |
Manufacturer Phone | 7635146694 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CARMEDA PEDIATRIC BIO-PROBE |
Generic Name | EXTRAVASCULAR BLOOD FLOW PROBE |
Product Code | DPT |
Date Received | 2003-02-20 |
Model Number | CBDP-38P |
Catalog Number | 95140 |
Lot Number | UNK |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 433404 |
Manufacturer | MEDTRONIC PERFUSION SYSTEMS |
Manufacturer Address | 7611 NORTHLAND DR. BROOKLYN PARK MN 55428 US |
Baseline Brand Name | CARMEDA PEDIATRIC BIO-PROBE |
Baseline Generic Name | EXTRAVASCULAR BLOOD PLOW PROBE |
Baseline Model No | CBDP-38P |
Baseline Device Family | FLOW PROBE |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 24 |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K891687 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2003-02-20 |