Magnetom Espree. Magnetic Resonance Imaging System. model number 10018165
FDA Recall Z-1529-05 · Posted 2005-09-09
Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLNN
Date Initiated2005-08-12
Date Terminated2006-07-19
Product Quantity209 units
Reason for Recall
there is a misalignment of the patient table that may occur between the patient table and the opening to the magnet bore
Firm Action
The recalling firm issued via certified mail a Customer Safety Advisory to the affected customers per Update Instructions MR031/05/S. the letter informs customers of the potential issue and provides instructions to avoid its occurrence.
Root Cause
Other
Distribution Pattern
The products were shipped to medical facilities and MRI facilities nationwide.
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.