Reported Aug 1, 2018 · Terminated

MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…

GE Medical Systems, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE Medical Systems, LLC · 3200 N Grandview Blvd · Waukesha, WI · 53188-1693

Is this the product you have?

  • MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic resonance scanner (previously cleared K041476) can be used to produce head and whole body magnetic resonance images that are high resolution high signal-to-noise ratio, with short scan times. The Signa¿ Excite MR system with Surgical Option is indicated for use as a diagnostic imaging device to produce axial sagittal, coronal and oblique images, spectroscopic images, and/or spectra, dynamic images of the internal structures and organs of the entire body, including, but not limited to, head, neck, TMJ, spine, breast, heart, abdomen, pelvis, joints, prostate, blood vessels, and musculoskeletal regions of the body. The images produced by the Signa Excite system with Surgical Option reflect the spatial distribution of protons (hydrogen nuclei) exhibiting magnetic resonance. These images and/or spectra when interpreted by a trained physician yield information that may assist in diagnosis. The GE Signa Excite system with Surgical Option can provide MR images at various stages of a surgical procedure, and provides the capability to transfer a patient to the MR system table directly from a surgical table, or patient transport system. Images can be obtained using the MR scanner body coil, or local surface coils, and tile surface coils used with the integrated system may / can accommodate sterile draping for surgical procedures.
Lot codes and dates
    • Model Numbers M8074SS
    • M8053SS
    • M0074SS
    • M0001SS
    • 5265300-7
    • 5265300-8
  • Serial Number (System ID Number)
    • 00000000000002 (602406IMR)
    • 4295404 (4295404MR11)
    • N/A (415UCBHMR3)
    • N/A (720848MR4)
    • 00000304124MR1 (904202MR8)
    • N/A (309655IMRI)
    • 4425007 (913588NMRW)
    • 00000000UA0117 (616267IMRI)
    • 00000000000003 (507284NMRV)
    • 4311497 (MR229054)
    • 4510086 (212636SIGNA3T)
    • 00000000UA0116 (330344MR750W)
    • UA0326 (614293MR9)
    • N/A (614RMHTMR1)
    • 4371613 (412692MR750W)
    • N/A (214820ITABLE)
    • 4250114 (409772MR6)
    • 4550641 (4550641MR11)
    • 4482037 (757388750WMR)
    • 00000012228M63 (608263MR4IOR)
    • 4356151 (414805IMR1)
    • 00000299229MR5 (AH5824MR01)
    • 00000012051M69 (AH5824SS01)
    • 00000021158M61 (MRHM0885)
    • 00000014131M67 (MRHM0323)
    • 00000018480M64 (MR307144MR6)
    • 4565719 (082427110075)
    • 00000013254M68 (082445160014)
    • 000000PTST0008 (082427040101)
    • 000000PTST0007 (082427050024)
    • 4596631 (082427310113)
    • 4409769 (082427140133)
    • 000000PTST0003 (CS1020MR01)
    • DUMFMI60885001 (CS1006MR03)
    • 00001309FMM07L (T4185506)
    • 00000021695M62 (M4194477)
    • 00000021695M62 (X41944020)
    • 00000305145MR5 (UC2547MR01)
    • 4320023 (083027822002316)
    • 4508956 (A5381507)
    • 00000010003M62 (EM0293)
    • 00001219FMM0H1 (EM0105)
    • 00000017217M61 (EM0105)
    • 000000PTST0010 (YM3833)
    • 00000000000004 (YM1733)
    • 2937140 (0850270414)
    • 4548529 (KW1008MR08)
    • 000000PTST0006 (ZA2169MR01)
    • 00001251FMM044 (34368MRS01)
    • 4344097 (34418MRS01)
    • 4605737 (N/A)
    • 000000PTST0005 (10590MRS01)
    • DUMFMI60885002 (10590MRS02)
    • 4569734 (00132MRS01)
Amount recalled
54 units total

Where it was sold

Why it was recalled

There is a potential safety issue with the table transfer release of the MR Surgical Suite System which may cause an unexpected loss of function of the patient transfer mechanism that allows the patient to be moved from the GE MR Surgical Table to the Maquet Magnus Surgical Table.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 29, 2024 · Data as of Sep 19, 6:51 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.