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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MERIT MEDICAL SINGAPORE PTE LTD. SAFEDRAW TRANSDUCER SET; BLOOD PRESSURE TRANSDUCER SET

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MERIT MEDICAL SINGAPORE PTE LTD. SAFEDRAW TRANSDUCER SET; BLOOD PRESSURE TRANSDUCER SET Back to Search Results
Model Number 682000
Device Problem Fluid/Blood Leak (1250)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 08/25/2021
Event Type  malfunction  
Manufacturer Narrative
The suspect device is expected to return for evaluation.A follow up will be submitted when the evaluation is complete.
 
Event Description
The account alleges that before use, the transducer showed signs of leaking.No patient consequence to report.
 
Manufacturer Narrative
The suspect device was not returned for evaluation.The complaint could not be confirmed.The root cause could not be determined.A search of the complaint database was performed and no similar complaints for this lot number were found.The device history record was reviewed, and no exception documents were found.
 
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Brand Name
SAFEDRAW TRANSDUCER SET
Type of Device
BLOOD PRESSURE TRANSDUCER SET
Manufacturer (Section D)
MERIT MEDICAL SINGAPORE PTE LTD.
198 yishun ave 7
singapore, 76892 6
SN  768926
MDR Report Key12548585
MDR Text Key274025519
Report Number8020616-2021-00060
Device Sequence Number1
Product Code DSK
UDI-Device Identifier00886333620005
UDI-Public00886333620005
Combination Product (y/n)N
PMA/PMN Number
K935782
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,foreig
Type of Report Initial,Followup
Report Date 09/01/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/29/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number682000
Device Catalogue Number682051/CNA
Device Lot NumberC2110518
Was Device Available for Evaluation? No
Date Manufacturer Received10/10/2021
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
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