VS200 WALLSTAND 110-5010G1

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-15 for VS200 WALLSTAND 110-5010G1 manufactured by Del Medical Inc..

Event Text Entries

[146653398] A corrective action investigation has been initiated and is still on-going.
Patient Sequence No: 1, Text Type: N, H10


[146653399] Bolt in counterweight sheared, cassette holder carriage was guided to the lower end of vertical travel by the technologist. No injuries reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1418964-2019-00016
MDR Report Key8516338
Date Received2019-04-15
Date of Report2019-04-15
Date of Event2018-10-18
Date Mfgr Received2018-10-18
Device Manufacturer Date2012-04-01
Date Added to Maude2019-04-15
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 FDA3
Event Location3
Manufacturer ContactMR. WILLIAM KOSTECKI
Manufacturer Street241 COVINGTON DRIVE
Manufacturer CityBLOOMINGDALE IL 60108
Manufacturer CountryUS
Manufacturer Postal60108
Manufacturer Phone8472887022
Manufacturer G1DEL MEDICAL INC.
Manufacturer Street241 COVINGTON DRIVE
Manufacturer CityBLOOMINGDALE IL 60108
Manufacturer CountryUS
Manufacturer Postal Code60108
Single Use3
Remedial ActionRP
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameVS200 WALLSTAND
Generic NameRADIOGRAPHIC CASSETTE HOLDER
Product CodeIXY
Date Received2019-04-15
Model NumberVS200
Catalog Number110-5010G1
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerDEL MEDICAL INC.
Manufacturer Address241 COVINGTON DRIVE BLOOMINGDALE IL 60108 US 60108


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-15

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