MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2000-11-27 for WINSTED * manufactured by Winsted Corp.
[199738]
Cart was used to hold video monitor. While moving the cart, one of the back wheels fell off. Nurse tried to stop the video monitor from crashing to the floor. This resulted in blunt trauma to both feet with abrasions to both shins and injury to two fingers on the right hand.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 306492 |
| MDR Report Key | 306492 |
| Date Received | 2000-11-27 |
| Date of Report | 2000-11-22 |
| Date of Event | 2000-11-01 |
| Date Facility Aware | 2000-11-01 |
| Report Date | 2000-11-22 |
| Date Added to Maude | 2000-12-01 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Reporter Occupation | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | WINSTED |
| Generic Name | CART |
| Product Code | LDQ |
| Date Received | 2000-11-27 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | C9292 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 296599 |
| Manufacturer | WINSTED CORP |
| Manufacturer Address | 10901 HAMPSHIRE AVE S MINNEAPOLIS MN 55438 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 1 | 1. Other | 2000-11-27 |