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Terminated

Magnetom Symphony/Sonata, OR Table.

FDA Recall Z-0976-03 · Posted 2003-07-03

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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