MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 2006-10-02 for D-STAT FLOWABLE HEMOSTAT 4000 * manufactured by Vascular Solutions, Inc..
[512181]
A hemodialysis catheter was removed from a patient's left internal jugular (ij) vein. While maintaining pressure on the left ij vein, the physician administered the d-stat flowable hemostat into the tissue tract of the left ij vein access site to control bleeding. The patient became unresponsive and "coded. " the patient later expired. No information is available at this time regarding the cause of death. Use of the d-stat flowable product in this manner represented an off-label use of the product.
Patient Sequence No: 1, Text Type: D, B5
[7804118]
The device was used for an unapproved indication.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2134812-2006-00016 |
| MDR Report Key | 766300 |
| Report Source | 05,06 |
| Date Received | 2006-10-02 |
| Date of Report | 2006-10-02 |
| Date of Event | 2006-09-15 |
| Date Mfgr Received | 2006-09-15 |
| Date Added to Maude | 2006-10-04 |
| 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 | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 0 |
| Manufacturer Contact | JULIE TAPPER |
| Manufacturer Street | 6464 SYCAMORE CT. |
| Manufacturer City | MINNEAPOLIS MN 55369 |
| Manufacturer Country | US |
| Manufacturer Postal | 55369 |
| Manufacturer Phone | 7636564228 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | D-STAT FLOWABLE HEMOSTAT |
| Generic Name | TOPICAL HEMOSTAT |
| Product Code | MHW |
| Date Received | 2006-10-02 |
| Model Number | 4000 |
| Catalog Number | * |
| Lot Number | 301228 |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 754178 |
| Manufacturer | VASCULAR SOLUTIONS, INC. |
| Manufacturer Address | * MINNEAPOLIS MN 55369 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Death | 2006-10-02 |