BUBBLE TRAP HOLDER 1XX*XH041 NA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 2011-09-20 for BUBBLE TRAP HOLDER 1XX*XH041 NA manufactured by Terumo Cardiovascular Systems, Corp..

Event Text Entries

[17962633] Terumo has not received the actual device for investigation; therefore, terumo is still investigating this issue, and a follow-up report will be submitted when the investigation is completed and more info becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[18043414] The user facility reported to terumo cardiovascular systems that during cardiopulmonary bypass surgery, it was noticed that the ring that holds the arterial filter was cracking. The product was not changed out. There was no pt injury. The surgery was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9681834-2011-00055
MDR Report Key2298561
Report Source05,06,07
Date Received2011-09-20
Date of Report2011-03-18
Date of Event2011-03-18
Date Facility Aware2011-03-18
Report Date2011-03-18
Date Mfgr Received2011-03-18
Date Added to Maude2012-05-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMICHAEL SILVESTRI, DIRECTOR
Manufacturer Street125 BLUE BALL RD.
Manufacturer CityELKTON MD 21921
Manufacturer CountryUS
Manufacturer Postal21921
Manufacturer Phone8002623304
Manufacturer G1TERUMO CARDIOVASCULAR SYSTEMS, CORP.
Manufacturer Street125 BLUE BALL RD.
Manufacturer CityELKTON MD 21921
Manufacturer CountryUS
Manufacturer Postal Code21921
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameBUBBLE TRAP HOLDER
Generic NameBUVVLE TRAP HOLDER
Product CodeKRL
Date Received2011-09-20
Model Number1XX*XH041
Catalog NumberNA
Lot NumberUNK
ID NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeNA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTERUMO CARDIOVASCULAR SYSTEMS, CORP.
Manufacturer Address125 BLUE BALL RD. ELKTON MD 21921 US 21921


Patients

Patient NumberTreatmentOutcomeDate
10 2011-09-20

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