MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-12-23 for LUMBAR DRAIN CATHETER CLOSED TIP 46419 manufactured by Medtronic.
[34760277]
Catheter tip sheared during lumbar drain procedure, retained, new catheter placed with good csf flow.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5058788 |
MDR Report Key | 5334194 |
Date Received | 2015-12-23 |
Date of Report | 2015-12-23 |
Date of Event | 2015-12-14 |
Date Added to Maude | 2015-12-30 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
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 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | LUMBAR DRAIN CATHETER CLOSED TIP |
Generic Name | VENTRICULOSTOMY |
Product Code | LKG |
Date Received | 2015-12-23 |
Model Number | 46419 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MEDTRONIC |
Manufacturer Address | MINNEAPOLIS MN 55432 US 55432 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-12-23 |