MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2005-07-26 for PROSORBA COLUMN 9798701 manufactured by Fresenius Hemocare.
[417414]
Pt developed neck swelling after their second prosorba column treatment. They were diagnosed with a deep vein thrombosis in their internal jugular vein at the site of a permcath that had been place for prosorba treatments. They were hospitalized, anticoagulated and the catheter was removed. They will receive no further prosorba treatment.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3032792-2005-00014 |
| MDR Report Key | 623047 |
| Report Source | 05 |
| Date Received | 2005-07-26 |
| Date of Report | 2005-07-26 |
| Date of Event | 2005-06-29 |
| Date Mfgr Received | 2005-06-30 |
| Device Manufacturer Date | 2004-09-01 |
| Date Added to Maude | 2005-07-29 |
| 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 | JOE WINSLOW |
| Manufacturer Street | 14715 NE 95TH ST, STE 100 |
| Manufacturer City | REDMOND WA 98052 |
| Manufacturer Country | US |
| Manufacturer Postal | 98052 |
| Manufacturer Phone | 7814029355 |
| Manufacturer G1 | FRESENIUS HEMOCARE |
| Manufacturer Street | 14715 NE 95TH ST, STE 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 | PROTEIN A IMMUNOADSORPTION |
| Product Code | LQQ |
| Date Received | 2005-07-26 |
| Model Number | 9798701 |
| Catalog Number | 9798701 |
| Lot Number | QKN001C |
| ID Number | * |
| Device Expiration Date | 2006-03-31 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | N |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 612695 |
| Manufacturer | FRESENIUS HEMOCARE |
| Manufacturer Address | * REDMOND WA * 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. Hospitalization | 2005-07-26 |