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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON S2000 ULTRASOUND SYSTEM ULTRASOUND DEVICE

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SIEMENS MEDICAL SOLUTIONS USA, INC. ACUSON S2000 ULTRASOUND SYSTEM ULTRASOUND DEVICE Back to Search Results
Model Number ACUSON S2000
Device Problem Device Emits Odor (1425)
Patient Problem Insufficient Information (4580)
Event Date 03/18/2016
Event Type  malfunction  
Event Description
As a result of this retrospective review, this mdr is being reported immediately upon discovery. It was reported that after a breast ultrasound procedure, the exam room smells like burning plastic after several hours of the system being turned on. There was no patient or user injury reported. No additional information was provided.
 
Manufacturer Narrative
Original submission narrative: this issue is under investigation. A follow-up report will be submitted when the investigation results are available. Follow-up narrative: this supplemental report is being submitted to update the device available for evaluation, update the follow-up type, update the device evaluated by manufacturer , update the event problem and evaluation codes, and provide the investigation results. Investigation: the root cause of the device problem could not be investigated because the defective system could not be returned. Because of the device not being returned, we were unable to confirm or reproduce the issue based on the information provided.
 
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Brand NameACUSON S2000 ULTRASOUND SYSTEM
Type of DeviceULTRASOUND DEVICE
Manufacturer (Section D)
SIEMENS MEDICAL SOLUTIONS USA, INC.
business area ultrasound
22010 se 51st street
issaquah WA 98029
MDR Report Key7789129
MDR Text Key281077492
Report Number3009498591-2016-00391
Device Sequence Number1
Product Code IYO
Combination Product (y/n)N
PMA/PMN Number
K140959
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,user f
Type of Report Initial
Report Date 08/27/2021
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received08/16/2018
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator
Device Model NumberACUSON S2000
Device Catalogue Number10041461
Device Lot NumberN/A
Was Device Available for Evaluation? No
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received03/25/2016
Is This a Reprocessed and Reused Single-Use Device? No

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