FDA Recall Terminated

RayStation Version 2.0.0.15, Radiation Therapy Treatment Planning System. RaySearch Laboratories AB Sveavagen 25, SE-111 34 Stockholm Sweden. [email protected] Designed for treatment planning and analysis of radiation therapy.

Recall: Z-1317-2012 · Initiated December 6, 2011

Recall

Recall Number
Z-1317-2012
Event Number
61269
Firm
RAYSEARCH LABORATORIES AB Sveavaegen 9 Stockholm Sweden
FEI Number
3007774465
Product Code
MUJ
Status
Terminated
Root Cause
Device Design
Initiated
December 6, 2011
Posted
March 26, 2012
Terminated
May 11, 2012

Description

RayStation Version 2.0.0.15, Radiation Therapy Treatment Planning System. RaySearch Laboratories AB Sveavagen 25, SE-111 34 Stockholm Sweden. [email protected] Designed for treatment planning and analysis of radiation therapy.

Reason

An issue was found with the dose calculation in the RayStation 2.0, that could result in a potential overestimation of the dose. This could lead to the potential under-dosage of a patient.

Action

The firm decided to recall and sent Urgent Field Safety Notice Medical Device Correction letters to consignees on 12/06/2011. The letters described the issue, identified the affected product, actions to be taken by the user, a solution, and contact information. Users are to follow the two part workaround, and educate their staff and all users on the workarounds. The letter states that the issue will be resolved in the next version of RayStation. If further information is needed, users are to contact either Freddie Cardel, Director of Customer Support, RaySearch Americas, at 1-877-778-3849 or [email protected]; or Niclas Borglund, Director of Service, RaySearch Laboratories AB, at 46-8-5450-6130 or [email protected]

Distribution

Worldwide Distribution -- US, including the states of FL, MA, NJ, and NY and the country of the Netherlands.

Quantity

21 units (16 domestically and 5 internationally)