ClearanceBrief
Recall Z-2251-2009 ยท MUJ System, Planning, Radiation Therapy Treatment

Brainlab AG

BrainLab Radiotherapy Treatment Planning Software; Catalog number 20610 - Radiosurgery 3.0 Catalog number 20620 - Radiosurgery 3.5 and Catalog number 20630 - Circular ARC SRS/SRT Planning. The software is intended for use in stereotactic, conformal, computer planned, LINAC based radiation treatment of cranial, head and neck, and extracranial lesions. It is intended to be used by experienced and

DateSep 20, 2009 (initiated Aug 12, 2009)
StatusTerminated
ReasonFailure to conduct important safety checks when using the BrainLab radiotherapy treatment planning software in combination with BrainLab conical collimators could result in unintended radiation outside the conical shaped field, which may lead to serious injury of the patient.
Root causeOther
ActionBrainLAB AG issued an "Urgent Field Safety Notice" letter dated August 12, 2009 informing all customers of the BrainLab radiotherapy planning software using conical collimators of the important safety checks to avoid the failure to apply and verify an adequate jaw-shaped field size and field position at the LINAC for the used conical collimator(s) or the failure to mount and verify the correct, intended conical collimator. Consignees were instructed on proper steps to take to avoid further issues. For further questions, contact BrainLAB AG by phone at 1-800-597-5911. *** On February 1, 2010
Quantity230 units
DistributionNationwide.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K002509NOVALIS (SHAPED BEAM SURGERY SYSTEM)
Brainlab AG, Nov 3, 2000
K080888MODEIFICATION TO IPLAN RT DOSE
Brainlab AG, Jun 11, 2008
K920879BRAINSCAN RADIOSURGERY MODULE
Brainlab, Dec 29, 1992
K994413BRAINSCAN
Brainlab AG, Jul 13, 2000