MagicView 1000 and Magic View Mondo. Digital Image Communication.
FDA Recall Z-0840-03 · Posted 2003-05-16
Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLMD
Date Initiated2003-07-03
Date Terminated2006-10-03
Product Quantity159 units
Reason for Recall
Potential error can occur with the 3D post processing options MPR, MIP, and VRT.
Firm Action
Siemens informed all users via a customer safety adv isory letter sent certified mail on 7/3/2002.
Root Cause
Other
Distribution Pattern
Units were distributed to hospitals and clinics throughout the nation. There are 11 government hospitals.
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.