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Terminated

Magnetom Trio TIM, magnetic resonance imaging

FDA Recall Z-0226-2007 · Posted 2006-11-29

Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLNH
Date Initiated2006-10-12
Date Terminated2008-04-23
Product Quantity9 units

Reason for Recall

Possible excessive RF exposure/may burn

Firm Action

The recalling firm has issued a Customer Safety Advisory to affected customers per Update Instructions MR038/06/S. The letter informs customers of the potential issue and instructs them not to use the involved coils until this issue can be corrected.

Root Cause

Other

Distribution Pattern

Nationwide.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K050200MAGNETOM TRIO A TIM SYSTEMSiemens Medical Solutions USA, Inc. · 2005-02-28

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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