MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 1995-07-07 for ELECTRIC PT LIFTER 622000 E-881 manufactured by Medi-man Rehab Products.
[16138045]
Nurse aide was transferring resident from bed to wheelchair with electrical pt lifter. In the process of transfer, the spreader bar on the lift broke, dropping the resident to the floor. Upon inspection it was determined that 2 welds had let loose, allowing the section of the spreader bar to fall apart. (*)
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1006432 |
| MDR Report Key | 23268 |
| Date Received | 1995-07-07 |
| Date of Report | 1995-06-26 |
| Date of Event | 1995-06-15 |
| Date Added to Maude | 1995-07-07 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ELECTRIC PT LIFTER |
| Generic Name | PT LIFTER |
| Product Code | FRZ |
| Date Received | 1995-07-07 |
| Model Number | 622000 E-881 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 23556 |
| Manufacturer | MEDI-MAN REHAB PRODUCTS |
| Manufacturer Address | MISSISSAUGA, ONTARIO CA L4W1P1 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 1995-07-07 |