Skip to content

Discovery MR450 recallZ-1188-2017 · GE Healthcare, LLC · initiated Jan 20, 2017

Class II Terminated All recalls posted in February 2017

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from GE Healthcare, LLC or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Potential safety issue with the patient bore heating on the Discovery MR450 narrow bore 1.5T MRI. In the event of a RF component failure, typically happening after extended system use, a small area on the bore surface may become warmer than normal. If this happens in an area where there is patient contact with the bore, and proper padding is not used, it may cause a serious burn.

FDA root cause category: Device Design

What the company is doing

The firm, GE Healthcare, sent an "URGENT MEDICAL DEVICE CORRECTION" letter GEHC Ref# 60913 Dated January 20, 2017. The letter was addressed to Hospital Administrators / Risk Managers, Radiology Department Managers & Radiologists. The letter described the Safety Issue, Safety Instructions, Affected Product Details, Product Correction & Contact Information. For questions contact GE Healthcare Service at 1-800-437-1171 or your local Service Representative.

Recall details

Recall number
Z-1188-2017
Recall class
Class II
Status
Terminated
Initiated by the company
Jan 20, 2017
Posted by the FDA
Feb 10, 2017
Recalling firm
GE Healthcare, LLC
Quantity
60
Product code
LNH
FDA submissions
K132376, K142085, K160618
Distribution
Worldwide Distribution- US (nationwide) including states of: CA, DC, IL, MN, MO, NY, SC, TX, WI, WV; and countries of: Canada, Czech Republic, Denmark, Finland, France, Germany, Italy, Netherlands, Norway, Poland, Saudi Arabia, Spain, Sweden, Switzerland, Taiwan, United Kingdom, and Uruguay.

Product description

Discovery MR450 The systems are whole body magnetic resonance scanners designed to support high resolution, high signal-to-noise ratio, and short scan times. It is indicated for use as a diagnostic imaging device to produce axial, sagittal, coronal, and oblique images, spectroscopic images, parametric maps. and/or spectra, dynamic images of the structures and/or functions 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.

Code information (models, lots, serial numbers)

Show the full code information (2k characters)

Mfg. Lot or Serial # System ID 00001106XF509E 209225VC450 00001106XF50A6 858939MR4 000000000R7216 858939MR3 000000000R2645 202715MR2 00000842BD50C2 202476MR1 000000000R7025 217383CMR5 00000944BD6155 MR129036 101BD66B6 573884MRI 00000945BD6182 417COXMR1 000000000R2768 HSSFMR450 00001009BD65C1 HSS75MR450 00000944BD6166 803434MRI 00000298722MR0 803434MR2 00000300039MR5 832522MR2 Not Available 713566SMITH1 1106xf508e 713566SMITH3 00000296429MR4 281364MR2 00000833BD4AE7 920830MR450 00000933BD5DF8 304256MR2 00000294451MR0 030020MR03 000000000R7320 403541MR1 00000944BD616B 403955MR1 000000000R7149 250727MR2 Not Available 905522MR2 00001101XF5028 514281MR450 00000297813MR8 CS1006MR04 00000294548MR3 DK1083MR06 00000294397MR5 FI1128MR01 00000295485MR7 FI1052MR01 00000296032MR6 A2032112 00000295847MR8 M4182438 00000293919MR7 M206565701 00000294575MR6 M40330108 00000298332MR8 RMUE01MR04 0002001-0917-3 A5127236 00000304354MR4 A5808528 00000296820MR4 A5624132 00000297807MR0 D5354206 00000293603MR7 RTD0127 DUMFMI60898001 NO1017MR03 00000297987MR0 NO1009MR02 00000296493MR0 PL1539MR01 00000300882MR8 SA1058MR02 00000296613MR3 SA1011MR03 00000299452MR3 CPZ43620 00000303993MR0 M001MR01 00000293000MR6 A010MR06 00000293920MR5 N002MR02 00000303992MR2 541010MR03 00000300849MR7 0853270113 00000292973MR5 00242MRS02 00000293206MR9 70001MRS09 00000298041MR5 05217MRS02 00000293642MR5 10448MRS02 00000293724MR1 10050MRS03 00000299340MR0 00010MRS01 00000295709MR0 00200MRS04 00000294967MR5 00100MRS01 00000296514MR3 00105MRS02 00000300689MR7 2948529MR

Other devices under the same FDA submission

13 devices cleared under K132376, K142085, K160618 — the recall does not name any of them by identifier. One submission often covers many models, so they may or may not be affected.

Sources and updates

How recalls are matched to devices · Editorial policy · Report an error on this page