MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-02 for SARNS 8000 PERFUSION SYSTEM 195215 manufactured by Terumo Cardiovascular Systems Corporation.
[81802485]
(b)(4). The fsr observed no visible damage to the sensor or cable. He installed a new level sensor. The unit operated to the manufacturer? S specifications. The suspect level sensor was returned to the manufacturer for further evaluation.
Patient Sequence No: 1, Text Type: N, H10
[81802486]
The field service representative (fsr) reported that during preventive maintenance (pm) of the device, the ultrasonic alert (yellow) level sensor intermittently shows "disconnected" light on the safety monitor when the level sensor cable was flexed. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1828100-2017-00338 |
| MDR Report Key | 6761669 |
| Date Received | 2017-08-02 |
| Date of Report | 2017-09-22 |
| Date of Event | 2017-07-10 |
| Date Mfgr Received | 2017-09-22 |
| Device Manufacturer Date | 2008-11-25 |
| Date Added to Maude | 2017-08-02 |
| 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 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. KATIE HOYT |
| Manufacturer Street | 6200 JACKSON ROAD |
| Manufacturer City | ANN ARBOR MI 48103 |
| Manufacturer Country | US |
| Manufacturer Postal | 48103 |
| Manufacturer Phone | 7346634145 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | SARNS 8000 PERFUSION SYSTEM |
| Generic Name | MONITOR AND/OR CONTROL, LEVEL SENSING, CARDIOPULMONARY BYPASS-SARNS 8000 |
| Product Code | DTW |
| Date Received | 2017-08-02 |
| Returned To Mfg | 2017-07-24 |
| Model Number | 195215 |
| Catalog Number | 195215 |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TERUMO CARDIOVASCULAR SYSTEMS CORPORATION |
| Manufacturer Address | 6200 JACKSON ROAD ANN ARBOR MI 48103 US 48103 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-08-02 |