MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2017-06-30 for S3 BUBBLE DETECTOR 23-07-40 manufactured by Livanova Deutschland.
[78957719]
Livanova (b)(4) manufactures the s3 bubble detector. The incident occurred in (b)(6). This medwatch report is being filed on behalf of livanova (b)(4). A livanova field service representative was dispatched to the facility to investigate. After communicating with the customer, the service representative learned that the actual issue that was experienced was the bubble sensor displayed 1/4", 3/8" and a yellow triangle at various points during a 5-day case. The service representative learned that the customer reset power to the s5 system, but it did not resolve the issue. The bubble module was then removed from the e/p pack and re-seated and the bubble sensor was opened and closed, but the issue persisted. The field service representative was unable to reproduce the reported issue during functional testing. The bubble sensor and the bubble module were replaced as a precaution and the system software was updated. Subsequent testing of the system was carried out without issue and the unit was returned to service. A review of the dhr did not identify any deviations or non-conformities relevant to the reported issue. If any additional information pertinent to the reported event is received, it will be provided in a supplemental report. Evaluated on site by livanova technician
Patient Sequence No: 1, Text Type: N, H10
[78957720]
Livanova (b)(4) received a report that the s3 bubble detector turned on and off intermittently during a procedure. There was no report of patient injury.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9611109-2017-00504 |
| MDR Report Key | 6681159 |
| Report Source | HEALTH PROFESSIONAL |
| Date Received | 2017-06-30 |
| Date of Report | 2017-06-30 |
| Date of Event | 2017-06-06 |
| Date Mfgr Received | 2017-06-06 |
| Device Manufacturer Date | 2013-10-23 |
| Date Added to Maude | 2017-06-30 |
| 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 | JOAN CEASAR |
| Manufacturer Street | 14401 W. 65TH WAY |
| Manufacturer City | ARVADA CO 80004 |
| Manufacturer Country | US |
| Manufacturer Postal | 80004 |
| Manufacturer Phone | 2812287260 |
| Manufacturer G1 | LIVANOVA DEUTSCHLAND |
| Manufacturer Street | LINDBERGHSTR. 25 |
| Manufacturer City | MUNICH 80939 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 80939 |
| Single Use | 3 |
| Remedial Action | OT |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | S3 BUBBLE DETECTOR |
| Generic Name | MONITOR AND/OR CONTROL, LEVEL SENSING, CARDIOPULMONARY BYPASS |
| Product Code | DTW |
| Date Received | 2017-06-30 |
| Model Number | 23-07-40 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | LIVANOVA DEUTSCHLAND |
| Manufacturer Address | LINDBERGHSTR. 25 MUNICH 80939 GM 80939 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-06-30 |