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Terminated

Radiation therapy system - Coherence Therapist System 2.1 equipped with Coherence Therapist RTT2.1 or Primeview 3i R2.1, part number 8147667. Medical charged particle Radiation therapy system, part of the firm's beam limiting device/accessory. The product provides data processing, and the SYNGO standard medical imaging platform to provide comprehensive oncology workflow solutions for radiation therapy.

FDA Recall Z-2103-2008 · Posted 2008-09-17

Recall StatusTerminated
Product CodeIYE
Date Initiated2008-05-15
Date Terminated2010-12-20

Reason for Recall

Software - Under certain circumstances, the portal image may be overwritten, which may lead to incorrect dosage.

Firm Action

An Urgent Medical Device Correction - Customer Safety Advisory Notice letter (TH014/08/S) was released on May 15, 2008. A new software patch is under construction and is planned for release in June 2008. If you have any questions contact Roland Betz at (925) 246-8407.

Root Cause

Software design

Distribution Pattern

Class II Recall - Product distribution information pending from firm.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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