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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ESAOTE SPA MYLABALPHA; DIAGNOSTIC ULTRASOUND SYSTEM

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ESAOTE SPA MYLABALPHA; DIAGNOSTIC ULTRASOUND SYSTEM Back to Search Results
Model Number 101740000
Device Problem Electrical /Electronic Property Problem (1198)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 02/21/2020
Event Type  malfunction  
Manufacturer Narrative
The ac inlet solder joint has been damaged by excessive mechanical stress exerted on the joint via the ac cord either by multiple plugging/unplugging or mechanical stress applied to the ac cord.
 
Event Description
Customer reported that they saw smoke coming out of the dc adapter.They immediately unplugged the cord and did not use it again.There were no injuries or other damage reported.
 
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Brand Name
MYLABALPHA
Type of Device
DIAGNOSTIC ULTRASOUND SYSTEM
Manufacturer (Section D)
ESAOTE SPA
via melen 77
genoa, 16152
IT  16152
Manufacturer Contact
massimo polignano
via di caciolle, 15
firenze, fi 50127
IT   50127
MDR Report Key10274264
MDR Text Key207008332
Report Number9611125-2020-00003
Device Sequence Number1
Product Code IYN
UDI-Device Identifier08056304450012
UDI-Public08056304450012
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K161359
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor
Reporter Occupation Other
Remedial Action Replace
Type of Report Initial
Report Date 07/14/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received07/14/2020
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number101740000
Device Catalogue NumberMODEL 7400
Was Device Available for Evaluation? Yes
Date Manufacturer Received05/03/2020
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured08/27/2014
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage N
Patient Sequence Number1
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