• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ST. JUDE MEDICAL, INC. EP-WORKMATE¿ SCU-SIGNAL CONDITIONING UNIT (AMPLIFIER), 120 CHANNEL; COMPUTER, DIAGNOSTIC, PROGRAMMABLE

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

ST. JUDE MEDICAL, INC. EP-WORKMATE¿ SCU-SIGNAL CONDITIONING UNIT (AMPLIFIER), 120 CHANNEL; COMPUTER, DIAGNOSTIC, PROGRAMMABLE Back to Search Results
Model Number 100019203
Device Problem Communication or Transmission Problem (2896)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Date 08/14/2019
Event Type  Injury  
Manufacturer Narrative
The investigation results will be provided in a subsequent submission.
 
Event Description
During a supraventricular tachycardia ablation procedure a cancellation occurred.Following patient prep, the amplifier was powered on and intermittent connection occurred.The amplifier and media converter were power cycled without resolution.The fiber optic and ethernet cables were replaced and the issue still did not improve.The procedure was cancelled with no adverse patient consequences.
 
Manufacturer Narrative
One workmate claris amplifier with was received.The workmate claris amplifier was powered on and successful communication was established with the test standard workmate claris computer.However, the communication dropped and an error ¿amplifier disconnected¿ message was received on the live screen of the workmate claris system indicating that the communication between the workmate claris system and the amplifier terminated unexpectedly.During the evaluation, the amplifier status was reviewed including the single board computer (sbc) temperature and voltage sensors.The amplifier status revealed fluctuating microprocessor core temperature that exceeded the predetermined limit during operation.As designed, the single board computer initiated a system shutdown as the microprocessor operating temperature approaching a predefined threshold.The device history record was reviewed to ensure that each manufacturing and inspection operation was performed.The review determined the process was performed and completed in accordance with abbott specifications and procedures.Based on the information provided to abbott and the evaluation performed, the returned amplifier intermittently loss communication with the work mate claris computer due to the single board computer (sbc) temperature fluctuation exceeding the predetermined limits.Using a test standard sbc, the communication tests was performed for several hours and no interrupted or loss of communication was observed.The root cause of the intermittent connection and subsequent cancelled procedure was isolated to an intermittent sbc board.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
EP-WORKMATE¿ SCU-SIGNAL CONDITIONING UNIT (AMPLIFIER), 120 CHANNEL
Type of Device
COMPUTER, DIAGNOSTIC, PROGRAMMABLE
Manufacturer (Section D)
ST. JUDE MEDICAL, INC.
one st. jude medical drive
st. paul MN 55117
MDR Report Key8950654
MDR Text Key156133093
Report Number2184149-2019-00157
Device Sequence Number1
Product Code DQK
UDI-Device Identifier05415067003119
UDI-Public05415067003119
Combination Product (y/n)N
PMA/PMN Number
K151911
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,health
Type of Report Initial,Followup
Report Date 09/17/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Model Number100019203
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer09/13/2019
Was the Report Sent to FDA? No
Initial Date Manufacturer Received 08/14/2019
Initial Date FDA Received08/30/2019
Supplement Dates Manufacturer Received09/16/2019
Supplement Dates FDA Received09/17/2019
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
-
-