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.
Class I - DangerousWhat Should You Do?
- Check if you have this product: 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)
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- GE Medical Systems, LLC
- Reason for Recall:
- 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.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
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.
Product Codes/Lot Numbers:
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)
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2527-2018
Related Recalls
Senographe Pristina, Pristina Serena, and Pristina Serena 3D. for screening and diagnostic mammography
GE Medical Systems
Some Senographe Pristina systems either have a missing or an incorrect X-Ray Warning label, which is a nonconformance to FDA Regulation 21 CFR ¿1020.30(j).
MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph, Model Number 2030360-001, Product Codes VU2 and VU4
GE Medical Systems
If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable. This is visible as a damaged sheath or exposed wires. If a damaged Acquisition Trunk Cable is not recognized and removed from service, the cable can overheat with continued use.
LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535
GE Medical Systems
The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.