MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2002-08-07 for SYNTHETIC SLING MESH 72403284 NA manufactured by American Medical Systems, Inc..
[21695854]
Sling removed due to infection.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2183959-2002-00053 |
| MDR Report Key | 409575 |
| Report Source | 05 |
| Date Received | 2002-08-07 |
| Date of Report | 2002-08-06 |
| Date of Event | 2002-07-31 |
| Date Mfgr Received | 2002-07-31 |
| Device Manufacturer Date | 2001-08-01 |
| Date Added to Maude | 2002-08-12 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | THERESE BOWKER, MDR CONTACT |
| Manufacturer Street | 10700 BREN ROAD WEST |
| Manufacturer City | MINNETONKA MN 55343 |
| Manufacturer Country | US |
| Manufacturer Postal | 55343 |
| Manufacturer Phone | 9529306624 |
| Manufacturer G1 | * |
| Manufacturer Street | * |
| Manufacturer City | * |
| Manufacturer Country | * |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | SYNTHETIC SLING MESH |
| Generic Name | SURGICAL MESH |
| Product Code | FHK |
| Date Received | 2002-08-07 |
| Model Number | 72403284 |
| Catalog Number | NA |
| Lot Number | 329548013 |
| ID Number | * |
| Device Expiration Date | 2002-08-10 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | NA |
| Device Eval'ed by Mfgr | N |
| Implant Flag | Y |
| Date Removed | V |
| Device Sequence No | 1 |
| Device Event Key | 398588 |
| Manufacturer | AMERICAN MEDICAL SYSTEMS, INC. |
| Manufacturer Address | 10700 BREN RD., WEST MINNETONKA MN 55343 US |
| Baseline Brand Name | SYNTHETIC SLING/MESH |
| Baseline Generic Name | SURGICAL MESH |
| Baseline Model No | 72403284 |
| Baseline Catalog No | NA |
| Baseline ID | * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Required No Informationntervention | 2002-08-07 |