MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2009-09-20 for PRISMAFLEX * manufactured by Gambro Renal Products, Inc..
[17061868]
Machine was alarming increased negative pressure. Lines flushed without difficulty. Machine continued to alarm therefore attempted to inverse the lines. Upon completion attempted to continue therapy and the screen was frozen. The filter then became clotted.
Patient Sequence No: 1, Text Type: D, B5
[17142592]
Machine was alarming increased negative pressure. Lines flushed without difficulty. Machine continued to alarm therefore attempted to inverse the lines. Upon completion attempted to continue therapy and the screen was frozen. The filter then became clotted.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1495499 |
| MDR Report Key | 1495499 |
| Date Received | 2009-09-20 |
| Date of Report | 2009-09-20 |
| Date of Event | 2009-09-01 |
| Report Date | 2009-09-20 |
| Date Reported to FDA | 2009-09-20 |
| Date Added to Maude | 2009-10-08 |
| 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, CRRT |
| Product Code | MQS |
| Date Received | 2009-09-20 |
| Model Number | PRISMAFLEX |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | Y |
| Device Age | 1 YR |
| 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 | 2009-09-20 |