MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2007-08-10 for * manufactured by Zimmer Orthopaedic Surgical Products.
[16837537]
The patient was pulling himself to bed from the stretcher with the use of the trapeze bar when all of a sudden the whole frame fell on the bed. Note: the s-bar clamps broke. The orthopedic technician was notified and the entire equipment was changed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 905386 |
| MDR Report Key | 905386 |
| Date Received | 2007-08-10 |
| Date of Report | 2007-08-10 |
| Date of Event | 2007-07-17 |
| Report Date | 2007-08-10 |
| Date Reported to FDA | 2007-08-10 |
| Date Added to Maude | 2007-08-31 |
| 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 | * |
| Generic Name | TRAPEZE, ORTHOPEDIC, BAR CLAMPS |
| Product Code | ILZ |
| Date Received | 2007-08-10 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | N |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 880241 |
| Manufacturer | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS |
| Manufacturer Address | 200 WEST OHIO AVENUE DOVER OH 44622 US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2007-08-10 |