MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-10-07 for KENDALL 7325 * manufactured by Kendall Co..
[344348]
When pas stockings were removed pt was noted to have bruising around both legs.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1033525 |
| MDR Report Key | 557008 |
| Date Received | 2004-10-07 |
| Date of Report | 2004-10-01 |
| Date of Event | 2004-09-28 |
| Date Added to Maude | 2004-12-02 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| 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 | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | KENDALL |
| Generic Name | PAS STOCKINGS |
| Product Code | DWL |
| Date Received | 2004-10-07 |
| Model Number | 7325 |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 546676 |
| Manufacturer | KENDALL CO. |
| Manufacturer Address | * MANSFIELD MA 02048 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2004-10-07 |