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 Dyhnatronics.
[74633136]
The therapist had a patient on the table. The therapist used the foot plate to raise the high/low table. Once she removed her foot, the table continued to rise. The patient was able to be removed from the table without injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5069575 |
MDR Report Key | 6547336 |
Date Received | 2017-05-03 |
Date of Report | 2017-05-03 |
Date of Event | 2017-05-03 |
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 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 | 0 |
Brand Name | ULTRA HIGH/LOW TABLE |
Generic Name | TABLE, POWERED |
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 | DYHNATRONICS |
Manufacturer Address | US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-05-03 |