MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2000-07-11 for MEDTRONIC TS 46442 * manufactured by Medtronic Ps Medical.
[149959]
Upon removal of external spinal drainage system, it was noted that 0. 5cm of the catheter tip was missing.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1019270 |
| MDR Report Key | 285561 |
| Date Received | 2000-07-11 |
| Date of Report | 2000-07-11 |
| Date of Event | 2000-06-10 |
| Date Added to Maude | 2000-07-14 |
| 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 | MEDTRONIC TS |
| Generic Name | EXTERNAL SPINAL DRAINAGE SYSTEM |
| Product Code | MAJ |
| Date Received | 2000-07-11 |
| Model Number | 46442 |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Implant Flag | Y |
| Date Removed | V |
| Device Sequence No | 1 |
| Device Event Key | 276349 |
| Manufacturer | MEDTRONIC PS MEDICAL |
| Manufacturer Address | 125 CREMONA DR UNIV BUSINESS CTR GOLETA CA 93117 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2000-07-11 |