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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: FUJIFILM HEALTHCARE CORPORATION ECHELON XL 1.5T MRI SYSTEM; SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING

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FUJIFILM HEALTHCARE CORPORATION ECHELON XL 1.5T MRI SYSTEM; SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING Back to Search Results
Model Number N/A
Device Problem Malposition of Device (2616)
Patient Problem Superficial (First Degree) Burn (2685)
Event Date 07/13/2023
Event Type  Injury  
Event Description
On (b)(6) 2023, fujifilm healthcare americas corporation became aware of an event involving echelon xl 1.5t mri system.It was reported that the patient complained of being burnt on her left wrist by the call bell cord during a scan of the lumbar spine.The patient experienced temporary redness/warming of the affected area and was observed at the facility.There were no visible signs of blistering and the patient was released without need for medical treatment or surgical intervention.There was no death associated with the event.
 
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Brand Name
ECHELON XL 1.5T MRI SYSTEM
Type of Device
SYSTEM, NUCLEAR MAGNETIC RESONANCE IMAGING
Manufacturer (Section D)
FUJIFILM HEALTHCARE CORPORATION
2-1 shintoyofuta
kashiwa-shi, chiba-ken 277-0 804
JA  277-0804
MDR Report Key17501333
MDR Text Key321049178
Report Number1528028-2023-00008
Device Sequence Number1
Product Code LNH
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 08/10/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/10/2023
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model NumberN/A
Device Catalogue NumberN/A
Device Lot NumberN/A
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Distributor Facility Aware Date07/13/2023
Event Location Hospital
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age22 YR
Patient SexFemale
Patient Weight91 KG
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