MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2009-09-30 for HOYER * manufactured by Joerns Healthcare, Inc..
[1176087]
Patient transferred from bed to cardiac chair. When transferring back to bed, the brake on the chair slipped and the patient almost landed on the floor. Staff believe brake was properly engaged.
Patient Sequence No: 1, Text Type: D, B5
[1181334]
Patient transferred from bed to cardiac chair. When transferring back to bed, the brake on the chair slipped and the patient almost landed on the floor. Staff believe brake was properly engaged.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1499301 |
| MDR Report Key | 1499301 |
| Date Received | 2009-09-30 |
| Date of Report | 2009-09-30 |
| Date of Event | 2009-07-07 |
| Report Date | 2009-09-30 |
| Date Reported to FDA | 2009-09-30 |
| Date Added to Maude | 2009-10-09 |
| 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 | HOYER |
| Generic Name | CHAIR, CARDIAC, POSTURE |
| Product Code | BYN |
| Date Received | 2009-09-30 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | NURSE |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | JOERNS HEALTHCARE, INC. |
| Manufacturer Address | 5001 JOERNS DR. STEVENS POINT WI 54481 US 54481 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2009-09-30 |