MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2002-07-10 for VESICA PERC STABILIZATION KIT WITH PROTEGEN SLING UNK manufactured by Microvasive Urology/a Division Of Boston Scientific Corp..
[276966]
The patient reported that subsequent to the implant of a protegen sling, patient experienced abdominal pain, vaginal erosion, infection in the sling area "and/or other physical complications". It is not known whether the device remains in the patient. The device was not returned for evaluation. Therefore, no failure analysis is available. Company's directions for use outline as potential complications: "tissue erosion... Infection... ".
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6000043-2002-00087 |
| MDR Report Key | 404472 |
| Report Source | 04 |
| Date Received | 2002-07-10 |
| Date of Report | 2002-06-12 |
| Date Reported to FDA | 2002-07-10 |
| Date Mfgr Received | 2002-06-12 |
| Date Added to Maude | 2002-07-16 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | JACK MOORE |
| Manufacturer Street | ONE BOSTON SCIENTIFIC PLACE |
| Manufacturer City | NATICK MA 017601537 |
| Manufacturer Country | US |
| Manufacturer Postal | 017601537 |
| Manufacturer Phone | 5086472594 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Remedial Action | RC |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VESICA PERC STABILIZATION KIT WITH PROTEGEN SLING |
| Generic Name | PERC STABILIZATION KIT |
| Product Code | FKH |
| Date Received | 2002-07-10 |
| Model Number | NA |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | NA |
| Device Eval'ed by Mfgr | R |
| Implant Flag | N |
| Date Removed | U |
| Device Sequence No | 1 |
| Device Event Key | 393468 |
| Manufacturer | MICROVASIVE UROLOGY/A DIVISION OF BOSTON SCIENTIFIC CORP. |
| Manufacturer Address | 780 BROOKSIDE DRIVE SPENCER IN 47460 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2002-07-10 |