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Richard Wolf GmbH · Model 5597101 · UDI-DI 04055207058848

OUG
1
510(k) clearances
2,980
Adverse events (10 deaths)
24
Recalls
315
Facilities

Description

CORE.PORTAL Establishes the connection between the intra-operative networks and the hospital-wide IT systems.Provides various services centrally in all operating rooms. Included are: Installation service Receiving and forwarding of patient lists by means of DICOM WORKLIST. Receiving and forwarding of images and videos by means of DICOM STORE. Intraoperative management of recorded images and videos using MEDIA ARCHIVE APP. A server, which provides the virtual environment with the ESXi operating system, is required for installation. The server hardware is not part of the Richard Wolf portfolio and must be provided by customers on their own.

Recalls

DateFirmReason
2023-03-08Radiometer Medical ApSDue to potential software issue that may result in patient mix-up information.
2023-02-06Biomerieux IncFor users with MYLA V4.8.X / V4.9 that use VITEK MS to identify organisms as part of their workflow, AST filter rules that have been activated are not always being applied to AST r
2021-09-02BioMerieux SAUnder certain conditions, there is a risk for a false negative result.
2020-09-22Pentax of America IncThere is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does
2020-09-22Pentax of America IncThere is an intermittent software issue that could affect the systems, in which an exam video for one patient (Patient A) might be copied to another patient (Patient B). This does
2020-01-17Beckman Coulter Inc.A security-only update was released via remote diagnostics on January 14, 2020 to customers with Windows 7 operation system. Shortly after the releases some customers reported that
2019-09-25ENDOTRONIXThe firm have received reports of patients myCordella Hubs fully powering themselves down without interaction from the patient or Endotronix.
2019-08-08Radiometer Medical ApSThe firm has become aware that there is a potential problem relating to the blood gas and immunoassay analyzer Systems that may result in patient mix-up when connected to some thir
2019-05-20Opternative IncLack of 510K clearance
2017-12-06Intel-GE Care Innovations LLCIt was discovered that in certain situations, including partial sessions and when taking adhoc measurements, the patient data was not synchronizing in a timely manner with the back

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.