MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2005-02-17 for ZIMMER UNK * manufactured by Zimmer Pt Care Div.
[393791]
When moving the pt's bed, the trapeze support broke causing it to fall and strike the pt's head.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW1034703 |
MDR Report Key | 575093 |
Date Received | 2005-02-17 |
Date of Report | 2005-02-17 |
Date of Event | 2005-02-14 |
Date Added to Maude | 2005-02-24 |
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 | ZIMMER |
Generic Name | TRAPEZE BAR |
Product Code | ILZ |
Date Received | 2005-02-17 |
Model Number | UNK |
Catalog Number | * |
Lot Number | * |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Implant Flag | N |
Date Removed | * |
Device Sequence No | 1 |
Device Event Key | 564940 |
Manufacturer | ZIMMER PT CARE DIV |
Manufacturer Address | 1872 OLD MOUNTAIN RD. STATESVILLE NC 28677 US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2005-02-17 |