MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2004-04-21 for GALILEO INTRAVASCULAR RADIOTHERAPY CARTRIDGE, SOURCE WIRE 1008112-0C NA manufactured by Guidant, Houston.
[312240]
The physicist reported the following scenario during a treatment: the site started to treat the first position in a two-position treatment. The system lost power during this treatment; therefore, the first position only received 1973 cgy dose. Instead of continuing this case, the oncologist repositioned the catheter to the second position and started a new two-position treatment. The second position received the normal 20 gy dose and then the system retracted to the third position and dwelled in this third position for a couple of seconds before the treatment. The second position received the normal 20 gy dose and then the system retracted to the third position and dwelled in this third position for a couple of seconds before the treatment was interrputed. This third area received a 56 cgy dose.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1651662-2004-00004 |
| MDR Report Key | 554040 |
| Report Source | 05,06,07 |
| Date Received | 2004-04-21 |
| Date of Report | 2004-03-26 |
| Date of Event | 2003-12-02 |
| Date Mfgr Received | 2004-03-26 |
| Device Manufacturer Date | 2000-07-01 |
| Date Added to Maude | 2004-11-10 |
| 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 | 3 |
| Reporter Occupation | PHYSICIST |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | DENISE VINMANS |
| Manufacturer Street | 26531 YNEZ RD |
| Manufacturer City | TEMECULA CA 92591 |
| Manufacturer Country | US |
| Manufacturer Postal | 92591 |
| Manufacturer Phone | 9099142050 |
| Manufacturer G1 | GUIDANT, HOUSTON |
| Manufacturer Street | 8934 KIRBY DR |
| Manufacturer City | HOUSTON TX 77054 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 77054 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | NA |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | GALILEO INTRAVASCULAR RADIOTHERAPY CARTRIDGE, SOURCE WIRE |
| Generic Name | RADIATION SYSTEM CARTRIDGE |
| Product Code | MOU |
| Date Received | 2004-04-21 |
| Returned To Mfg | 2004-01-09 |
| Model Number | 1008112-0C |
| Catalog Number | NA |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | NA |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 543667 |
| Manufacturer | GUIDANT, HOUSTON |
| Manufacturer Address | 8934 KIRBY DR HOUSTON TX 77054 US |
| Baseline Brand Name | GALILEO INTRAVASCULAR RADIOTHERAPY CARTRIDGE, SOURCE WIRE |
| Baseline Generic Name | RADIATION SYSTEM CARTRIDGE |
| Baseline Model No | 1008112-0C |
| Baseline Device Family | RADIATION SYSTEM CARTRIDGE |
| Baseline Shelf Life Contained | N |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | Y |
| Premarket Approval | P0000 |
| Baseline 510K PMN | N |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2004-04-21 |