3080 RL

MAUDE Adverse Event Report

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 .

Event Text Entries

[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


MAUDE Entry Details

Report Number7006391
MDR Report Key7006391
Date Received2017-11-07
Date of Report2017-09-20
Date of Event2017-07-19
Report Date2017-09-19
Date Reported to FDA2017-09-19
Date Reported to Mfgr2017-09-19
Date Added to Maude2017-11-07
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Generic NameHAND CONTROL, OPERATIONG TABLE
Product CodeFWY
Date Received2017-11-07
Model Number3080 RL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0


Patients

Patient NumberTreatmentOutcomeDate
10 2017-11-07

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