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 1999-03-24 for TRANSEND SHUTTLE 551555 manufactured by Sensor Medics Corp..
[164577]
The user of the transend shuttle reported that "it smoked". There was no pt involved and there were no injuries.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2050001-1999-00041 |
| MDR Report Key | 216736 |
| Report Source | 05,06,07 |
| Date Received | 1999-03-24 |
| Date of Report | 1999-03-24 |
| Date of Event | 1999-03-12 |
| Date Mfgr Received | 1999-03-12 |
| Date Added to Maude | 1999-04-01 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 0 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | TRANSEND SHUTTLE |
| Generic Name | CUTANEOUS GAS MONITOR |
| Product Code | LPP |
| Date Received | 1999-03-24 |
| Returned To Mfg | 1999-03-22 |
| Model Number | NA |
| Catalog Number | 551555 |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 210240 |
| Manufacturer | SENSOR MEDICS CORP. |
| Manufacturer Address | 22705 SAVI RANCH PKWY. YORBA LINDA CA 92887 US |
| Baseline Brand Name | CGS SHUTTLE (TRANSEND) |
| Baseline Generic Name | CUTANEOUS GAS MONITOR |
| Baseline Model No | NA |
| Baseline Catalog No | 551555 |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1999-03-24 |