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.
[74640358]
Therapist had a pt on the table. She went to raise the table using the foot plate and the table continued to rise even after removing her foot. The pt was unharmed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5069589 |
| MDR Report Key | 6547575 |
| Date Received | 2017-05-03 |
| Date of Report | 2017-05-03 |
| Date of Event | 2017-03-30 |
| 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 |