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Terminated

Magnetom Trio System. Nuclear Magnetic Resonance Imaging Diagnostic Device

FDA Recall Z-0521-04 · Posted 2004-02-10

Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLNH
Date Initiated2003-12-18
Date Terminated2004-11-09
Product Quantity16 units

Reason for Recall

tissue roll can become magnetic

Firm Action

The recalling firm has issued Updated Instructions to replace the stainless steel tissue roll holder. The recalling firm''s representatives are visiting each account to replace the tissue roll holder.

Root Cause

Other

Distribution Pattern

The product was shipped to medical facilities in CA, CT, DC, FL, GA, IL, IN, KS, KY, MA, MD, MN, NC, NY, OH, OR, PA, TX, and UT.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K013586MAGNETOM TRIO SYSTEMSiemens Medical Systems, Inc. · 2001-12-28

Official Source

View FDA Recall →

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

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