OPERON D850 3260.065

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2011-07-28 for OPERON D850 3260.065 manufactured by Berchtold Gmbh & Co. Kg.

Event Text Entries

[2174306] At the completion of a surgical procedure, the table top was reported to have dropped straight down between 6"-10" when the leg up button was pressed. The pt was caught by surgical personnel as the table dropped, and there was no pt injury reported.
Patient Sequence No: 1, Text Type: D, B5


[9288947] The table was evaluated by a berchtold corp. Service technician on (b)(4) 2011 after the incident at the location where the incident occurred. The table is in good physical condition. All the table functions operated as expected without problems, and the reported problem could not be duplicated. The table has been returned to the berchtold corporation facility in charleston, sc for further evaluation.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number8010153-2011-00002
MDR Report Key2239011
Report Source06
Date Received2011-07-28
Date of Report2011-07-22
Date of Event2011-06-28
Date Mfgr Received2011-06-28
Device Manufacturer Date2010-04-01
Date Added to Maude2012-06-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Manufacturer ContactCHRIS MANNARINO, U.S. AGENT
Manufacturer Street1950 HANAHAN ROAD
Manufacturer CityCHARLESTON SC 29406
Manufacturer CountryUS
Manufacturer Postal29406
Manufacturer Phone8002435135
Manufacturer G1BERCHTOLD GMBH
Manufacturer StreetLUDWIGSTALER STR. 25
Manufacturer CityTUTTLINGEN 78532
Manufacturer CountryGM
Manufacturer Postal Code78532
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOPERON
Generic NameSURGICAL TABLE
Product CodeFWY
Date Received2011-07-28
Model NumberD850
Catalog Number3260.065
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBERCHTOLD GMBH & CO. KG
Manufacturer AddressLUDWIGSTALER STR. 25 TUTTLINGEN GM


Patients

Patient NumberTreatmentOutcomeDate
10 2011-07-28

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