MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-07 for 3080 RL manufactured by .
[91502864]
Patient Sequence No: 1, Text Type: N, H10
[91502865]
Or table in labor and delivery reported not locking. Whenever the table is in the lowest position it does not move anymore. You have to bring it up by using the manual height switch then the table will start operating.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 7006391 |
MDR Report Key | 7006391 |
Date Received | 2017-11-07 |
Date of Report | 2017-09-20 |
Date of Event | 2017-07-19 |
Report Date | 2017-09-19 |
Date Reported to FDA | 2017-09-19 |
Date Reported to Mfgr | 2017-09-19 |
Date Added to Maude | 2017-11-07 |
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 |
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 |
Generic Name | HAND CONTROL, OPERATIONG TABLE |
Product Code | FWY |
Date Received | 2017-11-07 |
Model Number | 3080 RL |
Device Availability | * |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-11-07 |