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Terminated

MAGNETOM Verio Nuclear magnetic resonance imaging

FDA Recall Z-1401-2011 · Posted 2011-02-23

Recalling FirmSiemens Medical Solutions USA, Inc
Recall StatusTerminated
Product CodeLNH
Date Initiated2011-01-10
Date Terminated2012-09-25
Product Quantity92

Reason for Recall

On some systems the gradient cable connections did not meet firm's specifications after installation

Firm Action

Siemens Medical Solutions USA, Inc sent customers a letter on January 10, 2011 notifying them of an Update Instruction and informing them that recalling firm would preventatively check the gradient cable connections of all systems. For questions regarding this recall call 610-219-6300.

Root Cause

Other

Distribution Pattern

Nationwide Distribution including AK, AZ, CA, CT, FL, HI, IL, IN, KY, MA, MD, MI, MN, MO, MT, NC, NJ, NM, NV, OH, OK, OR, PA, RI, TN, TX, VA, WI, and WV

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K072237MAGNETOM VERIOSiemens Medical Solutions USA, Inc. · 2007-10-10

Official Source

View FDA Recall →

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

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