MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2007-01-08 for PROSORBA COLUMN 9798701 manufactured by Fresenius Hemocare.
[550688]
An ra patient developed right arm and hand swelling the evening after her 12th prosorba treatment. She was admitted to the hospital and diagnosed with thrombosis in her right internal jugular vein where her central venous catheter was (it was scheduled for removal the next day). She was treated with anticoagulants. The catheter removal was performed the next day and later that evening she developed dyspnea and chest pain. A ct then revealed bilateral pulmonary emboli. She was already on a heparin drip. She was discharged after 6 days.
Patient Sequence No: 1, Text Type: D, B5
[8051639]
This investigation is a clinical investigation only. Return of product not requested as evaluation of device after use not relevant to reported event. The device was used according to labeled indications and in the appropriate environment. Temporal relationship of the event of prosorba might suggest a contributory relationship because the patient would not have had this central venous catheter if she had not been undergoing treatments with prosorba.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 3032792-2007-00001 |
| MDR Report Key | 802843 |
| Report Source | 05 |
| Date Received | 2007-01-08 |
| Date of Report | 2007-01-05 |
| Date of Event | 2006-11-21 |
| Report Date | 2007-01-08 |
| Date Mfgr Received | 2006-12-10 |
| Device Manufacturer Date | 2005-07-01 |
| Date Added to Maude | 2007-01-12 |
| 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 |
| Reporter Occupation | MEDICAL TECHNOLOGIST |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | JOSHUA LASKER |
| Manufacturer Street | 14715 NE 95TH ST STE 100 |
| Manufacturer City | REDMOND WA 98052 |
| Manufacturer Country | US |
| Manufacturer Postal | 98052 |
| Manufacturer Phone | 4252422154 |
| 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 | IMMUNOADSORPTION COLUMN |
| Product Code | LQQ |
| Date Received | 2007-01-08 |
| Model Number | 9798701 |
| Catalog Number | 9798701 |
| Lot Number | RGN001D |
| ID Number | * |
| Device Expiration Date | 2007-01-31 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | 16 MO |
| Device Eval'ed by Mfgr | N |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 790347 |
| 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 | 2007-01-08 |