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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AVANOS MEDICAL SALES / AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.) BALLARD MULTI-ACCESS CATHETER; CATHETERS, SUCTION, TRACHEOBRONCHIAL

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AVANOS MEDICAL SALES / AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.) BALLARD MULTI-ACCESS CATHETER; CATHETERS, SUCTION, TRACHEOBRONCHIAL Back to Search Results
Model Number 1920
Device Problems Defective Component (2292); Obstruction of Flow (2423)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 01/31/2023
Event Type  malfunction  
Event Description
Intubated neonate required administration of surfactant.Nurse and respiratory therapist unable to administer the medication through the opening in the y-piece of the attachment.Y-piece with suction catheter attached to endotracheal tube was noted to have a defect, not allowing a suction catheter or medication to pass into the tube.The respiratory therapist was able to change the y-piece with one that did not have the defect and administer the surfactant.No harm to patient.
 
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Brand Name
BALLARD MULTI-ACCESS CATHETER
Type of Device
CATHETERS, SUCTION, TRACHEOBRONCHIAL
Manufacturer (Section D)
AVANOS MEDICAL SALES / AVANOS MEDICAL, INC. (FORMERLY HALYARD HEALTH INC.)
alpharetta GA 30004
MDR Report Key16502724
MDR Text Key310980505
Report NumberMW5115525
Device Sequence Number1
Product Code BSY
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Risk Manager
Type of Report Initial
Report Date 03/02/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number1920
Device Lot Number30193655
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received03/06/2023
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Age1 DA
Patient SexMale
Patient EthnicityNon Hispanic
Patient RaceWhite
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