MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-23 for CIRRUS 600 manufactured by Tollos.
[133860154]
The ceiling lift in the patient's room was about to be hooked up to the patient's sling in order to get the patient back to bed. The lift had been charging for approximately two hours prior to being used, since the battery was depleted. The lift would not move up or down when controls were pressed. When the nurse pushed the 'up' button, the lift suddenly dropped over a foot, almost hitting the patient in the head. The nurse grabbed the metal part of the lift and kept it from hitting the patient.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8270127 |
| MDR Report Key | 8270127 |
| Date Received | 2019-01-23 |
| Date of Report | 2018-12-18 |
| Date of Event | 2018-12-05 |
| Report Date | 2018-12-18 |
| Date Reported to FDA | 2018-12-18 |
| Date Reported to Mfgr | 2019-01-23 |
| Date Added to Maude | 2019-01-23 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| 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 | CIRRUS |
| Generic Name | LIFT, PATIENT |
| Product Code | FNG |
| Date Received | 2019-01-23 |
| Model Number | 600 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TOLLOS |
| Manufacturer Address | 8 EASTER CT STE J OWINGS MILLS MD 21117 US 21117 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-01-23 |