FDAFebruary 14, 2018device
ExacTrac versions 6.5 through 6.5 intended to be used to place patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures, in order to treat lesions, tumors and conditions anywhere in the body when radiation ...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
The usage of workflows that deviate from the recommended specifications in the User manual for ExacTrac Patient Positioning System (versions 6.0, 6.1, 6.2, 6.5) with Auxiliary Device Interface (ADI) and Varian Clinac or Varian TrueBeam, which may result in misinterpretation of beam authorization via ADI.
What to do
FDA enforcement status: Terminated
Brands named
brainlab agbrainlab
UPCs
0405648100026404056481138400
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDAOrigin Data Management software versions 3.1.0, 3.1.1, 3.1.2, 3.2.0, 3.2.12025-02-10
- FDACirq Arm System 2.02023-03-02
- FDABrainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.2023-02-14
- FDAExacTrac Dynamic software model numbers: 20910-01, ETD Positioning and Moni. 1.0.0 INST; 20910-01A, ETD Positioning and Moni. 1.0.1 INST; 20910-01B, ETD Positioning and Moni. 1.0.2 INST; and 20910-01C ETD Positioning and Moni. 1.0.3 INST.2022-02-25
- FDAExacTrac Dynamic software, Model 20910-01B ETD Positioning and Monitoring Installer 1.0.2 - Product Usage: intended to position patients at an accurately defined point within the treatment beam of a medical accelerator for stereotactic radiosurgery or radiotherapy procedures, to monitor the patie...2021-05-14
- FDAExacTrac Dynamic (Medical Charged-Particle Radiation Therapy System).2021-03-01
- FDAUltrasound Navigation Software 1.0 and Ultrasound Integration Software for Cranial/ENT Navigation 3.0.x and 3.1.x - Product Usage: intended to be an intra-operative image guided localization system to enable minimally invasive surgery.2020-08-31
- FDACirq Arm System - Model SBS 1.3.2 (Art.No. 56000-01B) and SBS 1.4 (Art.No. 56000-01C) of the CIRQ Arm System (56000 and 56000A)2020-08-20
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