MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-05-16 for PULSION PULSIOCATH THERMODILUTION CATHETERS PV2014L16N manufactured by Pulsion Medical Systems Se.
[108751489]
Further information surrounding the event has been sought. The involved guidewire was returned for investigation and investigation is ongoing. A supplemental medwatch report will be sent when the investigation is completed. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[108751490]
When (b)(6) applied the catheter on the patient, the guide wire stuck and became uncoiled. Catheter was replaced. Intramuscular bleeding occurred, but patient was not injured. (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3003263092-2018-00004 |
| MDR Report Key | 7519559 |
| Date Received | 2018-05-16 |
| Date of Report | 2018-07-20 |
| Date of Event | 2018-04-23 |
| Date Mfgr Received | 2018-04-23 |
| Date Added to Maude | 2018-05-16 |
| 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 Street | PULSION MEDICAL SYSTEMS SE HANS-RIEDL-STR. 21 |
| Manufacturer City | 85622 FELDKIRCHEN |
| Manufacturer Country | GM |
| Manufacturer Phone | 0498945991 |
| Manufacturer G1 | CHRISTINA KOEBERL |
| Manufacturer Street | PULSION MEDICAL SYSTEMS SE HANS-RIEDL-STR. 21 |
| Manufacturer City | 85622 FELDKIRCHEN |
| Manufacturer Country | GM |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | PULSION PULSIOCATH THERMODILUTION CATHETERS |
| Generic Name | PROBE, THERMODILUTION |
| Product Code | KRB |
| Date Received | 2018-05-16 |
| Returned To Mfg | 2018-05-14 |
| Model Number | PV2014L16N |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PULSION MEDICAL SYSTEMS SE |
| Manufacturer Address | PULSION MEDICAL SYSTEMS SE HANS-RIEDL-STR. 21 85622 FELDKIRCHEN GM |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-05-16 |