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Recall Observatory FDA recall evidence

Device product

Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic resonance diagnostic device (MRDD).

Z-1098-2016

February 10, 2016

Class II

Product summary

Firm
Deerfield Imaging
Event
Event 73421
Status
Terminated
Classification
Class II
Quantity
35 USA, 14 OUS
Official record key
device-enforcement:Z-1098-2016

Official wording

Reason: Emergency helium venting lines (i.e. quench lines) may not have been properly installed.

Code information: 70036, 10076-21, M00004, 10073-01, 23529, 40481, M00152, M00005, 30445, M00169, 060014, 10043-00, 30823, 10004680, 10050-01, 40662, 30935, 31084, 31203, 10002221, 40510, 40613, 30719, 31046, 30910, 30832, 30623, 31213, 10004152, 10072-01, 31250, 40815, 31049, 30068, 40412, M0038, M00106, M00367, 10035-01, 40475, 40495, 10007498, 10005946, 40263, 40688, 10058-00, 40619, 31085, and 10005639.

Distribution pattern: Worldwide Distribution -- US, including the states of CA, CT, FL, GA, IL, IN, MD, MA, MN, MO, NH, NC, OH, OR, PA, TX, UT, VA, and WI; and ,countries of CHINA, CANADA, AUSTRALIA, FRANCE, JAPAN, and GERMANY.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Emergency helium venting lines (i.e. quench lines) may not have been properly installed.