MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2000-03-01 for * 46420 manufactured by Medtronic Ps Medical.
[16266036]
When lumbar catheter was removed, it was found with approximately 1mm missing - not found.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1018306 |
| MDR Report Key | 266641 |
| Date Received | 2000-03-01 |
| Date of Report | 2000-02-02 |
| Date of Event | 2000-01-12 |
| Date Added to Maude | 2000-03-06 |
| 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 |
| Reporter Occupation | RISK MANAGER |
| 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 | * |
| Generic Name | LUMBAR CATHETER |
| Product Code | MAJ |
| Date Received | 2000-03-01 |
| Model Number | * |
| Catalog Number | 46420 |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 258132 |
| Manufacturer | MEDTRONIC PS MEDICAL |
| Manufacturer Address | 7000 CENTRAL AVE. MINNEAPOLIS MN 55432 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2000-03-01 |