Magnetom Symphony/Sonata, OR Table.
FDA Recall Z-0976-03 · Posted 2003-07-03
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Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLNH
Date Initiated2002-11-27
Date Terminated2004-05-11
Product Quantity2
Reason for Recall
OR Table stops during the transfer of the table to the MR system and will not move.
Firm Action
Customer Advisory Letter, number 01/2002 titled ''Potential Fault condition of the OR-Table in combination with Magnetom Symphony/Sonata' was sent out to the 2 hospitals in November, 2002.
Root Cause
Other
Distribution Pattern
CA, TX .
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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