HUT EXT DR FINAL ASSY-REVERSE 404007

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2011-12-22 for HUT EXT DR FINAL ASSY-REVERSE 404007 manufactured by Liebel-flarsheim Co.

Event Text Entries

[2429592] On (b)(6), customer reports the room failure was noted at start of days procedures. Customer does not have a back up room. Procedures were cancelled. No reported injury.
Patient Sequence No: 1, Text Type: D, B5


[9531207] Pending investigation. Upon receipt of investigation, a medwatch 3500a supplemental report will be submitted.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1518293-2011-00247
MDR Report Key2422632
Report Source05,06,07
Date Received2011-12-22
Date of Report2011-12-22
Date of Event2011-12-07
Date Mfgr Received2011-12-07
Device Manufacturer Date2006-11-01
Date Added to Maude2012-07-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactDAVID BENSON
Manufacturer Street2111 EAST GALBRAITH RD.
Manufacturer CityCINCINNATI OH 45237
Manufacturer CountryUS
Manufacturer Postal45237
Manufacturer Phone5139485719
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameHUT EXT DR FINAL ASSY-REVERSE
Generic NameUROLOGY SUITE
Product CodeKQS
Date Received2011-12-22
Model NumberHUT EXT DR
Catalog Number404007
Lot NumberNA
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerLIEBEL-FLARSHEIM CO
Manufacturer Address2111 EAST GALBRAITH RD. CINCINNATI OH 45237 US 45237


Patients

Patient NumberTreatmentOutcomeDate
10 2011-12-22

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.