Recall of Device Recall RayStation
Class 2 Device Recall RayStation 11B - accessdata.fda.gov
The notice was titled "Field Safety Notice, Medical Device Correction #99834." Customers were given precautions and instructed on a workaround. The issue will ...
Class 2 Device Recall RayStation
Class 2 Device Recall RayStation ; K200569 · System, planning, radiation therapy treatment25 - Product Code MUJ · RayStation standalone software radiation therapy ...
Recall of Device Recall Ray Station 2.0, 2.5, 3.0, 3.5 and 4.0
Raysearch laboratories has recalled "raysearch ray station 2.0, 2.5, 3.0, 3.5 and 4.0" software due to dose miscalculations for bolus/external/fixation support ...
Recall of Device Recall RayStation
Recall of Device Recall RayStation ; Event ID. 80252 ; Event Risk Class. Class 2 ; Event Number. Z-2290-2018 ; Event Initiated Date. 2018-03-28 ; Event Status. Open, ...
RayStation - Canada.ca - Recalls and Safety Alerts
An issue was found with the calculation of the reported SSD (i.e., the SSD displayed and exported) in RayStation RayPlan 7-2024a including ...
Medical Device Recalls in Radiation Oncology: Analysis of U.S. ...
Most recalls were for external beam devices (66.7%) and planning systems (22.9%), and recall events peaked in 2011. RODs differed significantly from other ...
Device Recalls. Information regarding device recalls and links to other device recall information may be ...
Info - S.2907 - 118th Congress (2023-2024): Medical Device Recall ...
All Info for S.2907 - 118th Congress (2023-2024): Medical Device Recall Improvement Act.
RayStation (2018-09-18) - Canada.ca - Recalls and Safety Alerts
Medical Device Recall; Subcategory: Medical Device; Hazard classification ... Affected products. RayStation. Reason. Issue found with robust optimization in ...
System for Australian Recall Actions - details
Medical Device · RC-2024-RN-00269-1 · RayStation RayPlan 7 through 2024A including some service packs. Multiple Products ARTG 195288 (Emergo Asia Pacific Pty Ltd ...
Medical Device Recalls News | MedTech Dive
Hologic has recalled the Biozorb devices after 188 reports of adverse events in patients who received the implants in breast tissue. By Susan Kelly • Oct. 28, ...
System for Australian Recall Actions - details
Medical Device · RC-2020-RN-00007-1 · Various RayStation and RayPlan Systems RayStation 4.0 RayStation 4.3(InverseArc) RayStation 4.5 RayStation 4.7 RayStation ...
Recall - RayStation Radiation Treatment Planning Sys - SoftwareCPR
IRAYSEARCH LABORATORIES AB, Stockholm, Sweden on 3/22/2018. Voluntary: Firm Initiated recall is ongoing. VOLUME OF PRODUCT IN COMMERCE 728.
RaySearch Laboratories: Software in radiation therapy and oncology
RaySearch is a world leader in software for radiation therapy. Our expertise supports 2600 clinics worldwide in the fight against cancer. Learn how.
Rayplan and Raystation - Recall Monitor
Health product recall: Rayplan and Raystation. Visit for more details and learn what to do.
GE Healthcare MRI Recall Update
This U.S. FDA notice was not related to any manufacturing defect or product-related error. It was a case of human error on site, and is in response to a single ...
RaySearch Labs issues urgent field safety notice for certain ...
RaySearch Labs issues urgent field safety notice for certain RayStations ... RaySearch Laboratories issued an urgent field safety notice in Europe ...
Urgent Field Safety Notice for RayStation by RaySearch ... - BfArM
For further information as well as details concerning the device please see the enclosed Advisory Notice of the manufacturer.
Appendix F. MAUDE and Medical Device Recall Reports
30037682. 77-2021-. 10020. 2021/04/27 Injury PHILIPS. ELECTRONICS. NEDERLAND. B.V.. 2021/05/26 LNH. INGENIA. 1.5T. Adverse. Event. Without.
Class 2 Device Recall Mindray BeneVision Distributed Monitoring ...
Action. Mindray issued URGENT Medical Device Correction letter on February 22, 2021 via certified mail, return receipt, signature required.