MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2004-10-01 for PROSORBA COLUMN 9798701 manufactured by Fresenius Hemocare, Inc..
[15187923]
Pt admitted to hosp with chest discomfort 4 days after 1st prosorba and diagnosed with staphylococcal aureus sepsis likely from their venous catheter. Treated with iv antibiotics and discharged after 7 days. No further prosorba to be done.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3032792-2004-00009 |
| MDR Report Key | 547442 |
| Report Source | 05 |
| Date Received | 2004-10-01 |
| Date of Report | 2004-10-01 |
| Date of Event | 2004-09-06 |
| Date Facility Aware | 2004-09-09 |
| Date Mfgr Received | 2004-09-09 |
| Device Manufacturer Date | 2004-03-01 |
| Date Added to Maude | 2004-10-08 |
| 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 | 0 |
| Manufacturer Contact | KAREN QUARFORD |
| Manufacturer Street | 14715 NE 95TH ST, SUITE 100 |
| Manufacturer City | REDMOND WA 98052 |
| Manufacturer Country | US |
| Manufacturer Postal | 98052 |
| Manufacturer Phone | 4252422154 |
| Manufacturer G1 | FRESENIUS HEMOCARE, INC. |
| Manufacturer Street | 14715 NE 95TH ST, SUITE 100 |
| Manufacturer City | REDMOND WA 98052 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 98052 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PROSORBA COLUMN |
| Generic Name | IMMUNOADSORPTION COLUMN |
| Product Code | LQQ |
| Date Received | 2004-10-01 |
| Model Number | 9798701 |
| Catalog Number | 9798701 |
| Lot Number | QCN002B |
| ID Number | * |
| Device Expiration Date | 2005-09-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Implant Flag | N |
| Date Removed | U |
| Device Sequence No | 1 |
| Device Event Key | 536850 |
| Manufacturer | FRESENIUS HEMOCARE, INC. |
| Manufacturer Address | 14715 NE 95TH ST. SUITE 100 REDMOND WA 98052 US |
| Baseline Brand Name | PROSORBA COLUMN |
| Baseline Generic Name | THERAPEUTIC PLASMA EXCHA |
| Baseline Catalog No | 9798701 |
| Baseline Device Family | PROTEIN A IMMUNOADSORPTION COL |
| Baseline Shelf Life Contained | Y |
| Baseline Shelf Life [Months] | 12 |
| Baseline PMA Flag | Y |
| Premarket Approval | P8500 |
| Baseline 510K PMN | N |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Life Threatening | 2004-10-01 |