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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MAQUET CARDIOVASCULAR LLC T.W. POWER SUPPLY; UNIT, CAUTERY, THERMAL, AC-POWERED

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MAQUET CARDIOVASCULAR LLC T.W. POWER SUPPLY; UNIT, CAUTERY, THERMAL, AC-POWERED Back to Search Results
Model Number T.W. POWER SUPPLY
Device Problems Failure to Deliver Energy (1211); Insufficient Information (3190)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 10/14/2021
Event Type  malfunction  
Event Description
The hospital reported that during preparation for an endoscopic vein harvesting procedure, t.W.Power supplys/n (b)(4) was sent to biomed not working.Warranty expired 05/17/2018.Service manual was requested and provided to hospital.
 
Manufacturer Narrative
Trackwise id # (b)(4).The device has not yet been returned to maquet cardiac surgery for evaluation.We are following up with the customer for the return of the device.A supplemental report will be submitted if the device is received.Device not returned.
 
Manufacturer Narrative
Trackwise id (b)(4).Updated sections: b5 - event description updated, g4, g7, h2, h10, h11.Corrected sections: h6 - health effect code changed; medical device code changed.The device has not yet been returned to maquet cardiac surgery for evaluation.We are following up with the customer for the return of the device.A supplemental report will be submitted if the device is received.
 
Event Description
The hospital reported that during preparation for an endoscopic vein harvesting procedure, t.W.Power supply (b)(6) was sent to biomed not working.Warranty expired 05/17/2018.Failure to deliver energy.Service manual was requested and provided to hospital.No patient effects.
 
Manufacturer Narrative
Trackwise (b)(4).Updated sections: g4, g7, h2, h6, h10.Analysis of production for oem devices: (3331/213/67) the reported device is an oem device.The certificate of conformance was reviewed for the reported serial number.The vendor certifies that this device serial number conforms to all applicable product specifications and there were no non-conformances identified for the manufacturing batch.Historical data analysis: (4109/213/67) the review of the historical data indicates that no other similar complaints was reported for the same serial number and reported failure mode.Trend analysis: (4110/213/67) the overall 24 month product complaint trend data for the period nov 2019 through oct 2021 was reviewed.There were no triggers identified for the review period.Communication/interviews: (4111/213/67) communication/interviews were performed to obtain all possible information.Device not returned: (4114/3221/67) despite request and/ or customer indicated that the device would be returned; however, no device was returned.
 
Event Description
N/a.
 
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Brand Name
T.W. POWER SUPPLY
Type of Device
UNIT, CAUTERY, THERMAL, AC-POWERED
Manufacturer (Section D)
MAQUET CARDIOVASCULAR LLC
45 barbour pond drive
wayne NJ
Manufacturer (Section G)
MAQUET CARDIOVASCULAR LLC
45 barbour pond drive
wayne NJ
Manufacturer Contact
arelean guzman
45 barbour pond drive
wayne, NJ 
MDR Report Key12761866
MDR Text Key281285523
Report Number2242352-2021-00910
Device Sequence Number1
Product Code HQO
UDI-Device Identifier00607567700826
UDI-Public00607567700826
Combination Product (y/n)N
PMA/PMN Number
K052274
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional,User Facility,Company Representative
Reporter Occupation Other
Type of Report Initial,Followup,Followup
Report Date 01/20/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/07/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model NumberT.W. POWER SUPPLY
Device Catalogue NumberC-VH-3010
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received01/21/2022
Was Device Evaluated by Manufacturer? No
Date Device Manufactured05/05/2017
Is the Device Single Use? No
Type of Device Usage Unknown
Patient Sequence Number1
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