MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1998-10-20 for CRAGG MACNAMARA VALVED INFUSION CATHETER * 201-0217 manufactured by Micro Therapeutics Inc..
[19494449]
Distal ring of cragg-macnamara 5 french infusion catheter dislodged during removal from a gortex-hemodialysis graft embolized into the radial artery.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW1014786 |
MDR Report Key | 192735 |
Date Received | 1998-10-20 |
Date Added to Maude | 1998-10-23 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 0 |
Report to FDA | 0 |
Event Location | 3 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CRAGG MACNAMARA VALVED INFUSION CATHETER |
Generic Name | INFUSION CATHETER |
Product Code | JCY |
Date Received | 1998-10-20 |
Model Number | * |
Catalog Number | 201-0217 |
Lot Number | * |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 187278 |
Manufacturer | MICRO THERAPEUTICS INC. |
Manufacturer Address | 1062-F CALLE NEGOCIO SAN CLEMENTE CA 92673 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1998-10-20 |