MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-01 for GOLVO 7007ES manufactured by Liko Ab (hill-rom Inc.).
[81484297]
Patient Sequence No: 1, Text Type: N, H10
[81484298]
The golvo lift stopped working while patient was in the sling, being moved to wheelchair after radiation treatment. We were able to use the emergency release to get him safely to his chair.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 6756381 |
| MDR Report Key | 6756381 |
| Date Received | 2017-08-01 |
| Date of Report | 2017-07-28 |
| Date of Event | 2017-07-27 |
| Report Date | 2017-07-28 |
| Date Reported to FDA | 2017-07-28 |
| Date Reported to Mfgr | 2017-07-28 |
| Date Added to Maude | 2017-08-01 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | GOLVO |
| Generic Name | LIFT, PATIENT, AC-POWERED |
| Product Code | FNG |
| Date Received | 2017-08-01 |
| Model Number | 7007ES |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | LIKO AB (HILL-ROM INC.) |
| Manufacturer Address | 1069 STATE ROUTE 46 EAST BATESVILLE IN 47006 US 47006 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-08-01 |