MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2009-10-10 for PRISMAFLEX * manufactured by Gambro Renal Products, Inc.
[21400073]
Patient receiving cvvhfd (continuous veno-venous hemodiafiltration) on new prismaflex crrt machine. Placed machine in recirculate mode so patient could go on road trip. When machine in recirculate mode it began alarming various alarms: unable to detect return pressure, effluent bag volume changing, blood pump malfunction, and blood detected in line.
Patient Sequence No: 1, Text Type: D, B5
[21427005]
Patient receiving cvvhfd (continuous veno-venous hemodiafiltration) on new prismaflex crrt machine. Placed machine in recirculate mode so patient could go on road trip. When machine in recirculate mode it began alarming various alarms: unable to detect return pressure, effluent bag volume changing, blood pump malfunction, and blood detected in line.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1516366 |
| MDR Report Key | 1516366 |
| Date Received | 2009-10-10 |
| Date of Report | 2009-10-10 |
| Date of Event | 2009-09-10 |
| Report Date | 2009-10-10 |
| Date Reported to FDA | 2009-10-10 |
| Date Added to Maude | 2009-10-27 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PRISMAFLEX |
| Generic Name | HEMODIALYSIS MACHINE, CRRT |
| Product Code | MQS |
| Date Received | 2009-10-10 |
| Model Number | PRISMAFLEX |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | NURSE |
| Device Availability | Y |
| Device Age | 6 MO |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | GAMBRO RENAL PRODUCTS, INC |
| Manufacturer Address | 14143 DENVER WEST PARKWAY, SUI LAKEWOOD CO 80401 US 80401 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2009-10-10 |