MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-03 for ULTRA HIGH/LOW TABLE manufactured by Dynatronics.
[74637146]
The pt was on the ultra by dynatronics table and the therapist used the footplate to raise the table. After the release of the foot plate, the table continued to raise on it's own. The therapist had to unplug the table in order to get it to stop. The pt was unharmed during this incident. The use of the table was discontinued and service was called to look at the table.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5069588 |
| MDR Report Key | 6547567 |
| Date Received | 2017-05-03 |
| Date of Report | 2017-05-03 |
| Date of Event | 2017-01-30 |
| Date Added to Maude | 2017-05-05 |
| 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 | 3 |
| Reporter Occupation | OTHER CAREGIVERS |
| 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 | 0 |
| Brand Name | ULTRA HIGH/LOW TABLE |
| Generic Name | POWERED TABLE |
| Product Code | INQ |
| Date Received | 2017-05-03 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | DYNATRONICS |
| Manufacturer Address | US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-05-03 |