MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-25 for LIKORALL 242 LILORALL 242 manufactured by Hill-rom, Inc..
[184867371]
Overhead lift carriage pin sheared and lift is not functional. Lift system was involved in a patient fall.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9877015 |
| MDR Report Key | 9877015 |
| Date Received | 2020-03-25 |
| Date of Report | 2020-02-21 |
| Date of Event | 2020-02-12 |
| Report Date | 2020-02-21 |
| Date Reported to FDA | 2020-02-21 |
| Date Reported to Mfgr | 2020-03-25 |
| Date Added to Maude | 2020-03-25 |
| 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 | RISK MANAGER |
| 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 | LIKORALL 242 |
| Generic Name | LIFT, PATIENT, CEILING MOUNTED |
| Product Code | FNG |
| Date Received | 2020-03-25 |
| Model Number | LILORALL 242 |
| Device Availability | Y |
| Device Age | 12 YR |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | HILL-ROM, INC. |
| Manufacturer Address | 1069 STATE ROUTE 46 EAST BATESVILLE IN 47006 US 47006 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-25 |