FDA Recall Terminated

Hitachi CXR-4 CT Computed Tomography X-ray System (including SceptreP3 PET/CT)

Recall: Z-1078-06 · Initiated February 21, 2006

Recall

Recall Number
Z-1078-06
Event Number
35081
Firm
Hitachi Medical Systems America Inc
FEI Number
1528028
Product Code
JAK
Status
Terminated
Root Cause
Other
Initiated
February 21, 2006
Posted
June 3, 2006
Terminated
November 13, 2008
Address
1959 Summit Commerce Park, Twinsburg, OH, 44087-2371

Description

Hitachi CXR-4 CT Computed Tomography X-ray System (including SceptreP3 PET/CT)

Reason

The device has a software anomaly which affects the system's ability to create Multiplanar Reconstructions (MPR). Some images from the resulting series do not display correctly, or display at all, when MPR was run on them.

Action

Hitachi Medical Systems America, Inc. became aware of an intermittent problem in the Multi-planar Reconstruction process when covering long ranges that could result in blank frames in the displayed reconstructions. HMSA also discovered a second software-related problem with the 50mm scale displayed on filmed images. In cases where the image has been magnified before filming, the 50mm scale is not correctly sized to the magnified image. Software corrections have already been installed on all units in order to correct the first of these problems (MPRs). According to the firm''s Device Notification Letter issued on 2/21/2006, a second software upgrade [which the firm states address both issues] will be released on or before 2/27/2006 and this correction will be performed by HMSA''s service personnel during each customer''s next scheduled PM. The Device Notification Letter also instructs the customers to call their Field Service Representatives or the HMSA Applications Helpline if they have any questions about the notice, or if any additional problems are encountered.

Distribution

The recalled MRI systems were distributed throughout the continental United States.

Quantity

15 units