BIGGER BETTER BLADDER BBB38

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-06-27 for BIGGER BETTER BLADDER BBB38 manufactured by Circulatory Technology Inc..

Event Text Entries

[48214725]
Patient Sequence No: 1, Text Type: N, H10


[48214726] Pump began alarming with an acute high negative bladder pressure of >-100 and pump was alarming. It was noted the better bladder was sucked into itself with very little blood in it. A 1. 1l volume was given to the pt and bladder remained concave. Air was aspirated from the hard shell case that encases the bladder in an attempt to expand it. It took approximately 240ml of air aspiration to get the bladder to open up. There was no air in the actual circuit. Pump began running at a higher flow but bladder continued to collapse multiple times. It was later determined there was a crack in the hard shell that was allowing air to be sucked in around the bladder. The leak was in a seam back to the inter chamber and outer housing. This caused the bladder to collapse. Manufacturer response for ecmo bladder, bigger better bladder (per site reporter): the manufacturer is in touch with a member of the fda and hospital staff.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number5750582
MDR Report Key5750582
Date Received2016-06-27
Date of Report2016-06-15
Date of Event2016-05-15
Report Date2016-06-15
Date Reported to FDA2016-06-15
Date Reported to Mfgr2016-06-15
Date Added to Maude2016-06-27
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag0
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIGGER BETTER BLADDER
Generic NameRESERVOIR, BLOOD, CARDIOPULMONARY BYPASS
Product CodeDTN
Date Received2016-06-27
Model NumberBBB38
Catalog NumberBBB38
Lot Number014603
Device Expiration Date2016-08-26
Device AvailabilityN
Device Age1 DY
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCIRCULATORY TECHNOLOGY INC.
Manufacturer Address21 SINGWORTH ST. OYSTER BAY NY 11771 US 11771


Patients

Patient NumberTreatmentOutcomeDate
10 2016-06-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.