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Recall Observatory FDA recall evidence

Device product

ExacTrac Vero is a Patient Positioning System for Radiation therapy.

Z-1929-2016

May 04, 2016

Class II

Product summary

Firm
Brainlab AG
Event
Event 74265
Status
Terminated
Classification
Class II
Quantity
27 Systems
Official record key
device-enforcement:Z-1929-2016

Official wording

Reason: Potentially incorrect positioning when using Implanted Marker Detection with Brainlab ExacTrac Vero 3.5

Code information: Potentially affected is ExacTrac Vero version 3.5 (including all subversions). Serial numbers/lot numbers are not applicable for a software version. Model/catalogue numbers: 20892 EXACTRAC VERO SOFTWARE 3.5 20892A EXACTRAC VERO SOFTWARE 3.5.1 20892B EXACTRAC VERO SOFTWARE 3.5.2 20892C EXACTRAC VERO SOFTWARE 3.5.3 20893 VERO INFRARED POSITIONING/MONITORING SW 46213 EXACTRAC VERO SW UPDATE 3.5 TO 3.5.1 46214 EXACTRAC VERO UPGRADE KIT 3.2 to 3.5 FOC 46215 EXACTRAC VERO UPGRADE KIT 3.1 TO 3.5 FOC 46216 EXACTRAC VERO SW UPDATE 3.5.2 TO 3.5.3 46228 EXACTRAC VERO 3.5 ROW 46238 EXACTRAC VERO 3.5 JAPAN

Distribution pattern: Distributed in the states of Florida, New York, Texas and Ohio, and in the countries of Belgium, France, Germany, Italy, Japan and South Korea.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potentially incorrect positioning when using Implanted Marker Detection with Brainlab ExacTrac Vero 3.5