TITAN STABILIZER ATTACHMENT T401231 N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-08-20 for TITAN STABILIZER ATTACHMENT T401231 N/A manufactured by Terumo Cardiovascular Systems Corporation.

Event Text Entries

[159599497] Terumo has not received the device for evaluation; therefore, the investigation has yet to be completed. Terumo plans on submitting a follow-up report when the investigation is complete and when more information becomes available. (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[159599498] The user facility reported to terumo cardiovascular that during cardiopulmonary bypass, the stabilizer's base got fractured when the doctor was adjusting it to attach to the patient. It is unknown if there was a blood loss in the procedure. Due to the unknown information for this event, it is being reported. Terumo continues to attempt to gain more information regarding this event from the user facility. No known impact or consequence to patient. Product was changed out. Procedure was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1124841-2019-00230
MDR Report Key8910584
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-08-20
Date of Report2019-09-18
Date of Event2019-07-29
Date Mfgr Received2019-09-12
Date Added to Maude2019-08-20
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. CATHLEEN HARGREAVES
Manufacturer Street125 BLUE BALL ROAD
Manufacturer CityELKTON MD 21921
Manufacturer CountryUS
Manufacturer Postal21921
Manufacturer Phone8002837866
Manufacturer G1SAME
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTITAN STABILIZER ATTACHMENT
Generic NameUNIVERSAL STABILIZER ARM
Product CodeMSW
Date Received2019-08-20
Returned To Mfg2019-08-27
Model NumberT401231
Catalog NumberN/A
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerTERUMO CARDIOVASCULAR SYSTEMS CORPORATION
Manufacturer Address125 BLUE BALL ROAD ELKTON MD 21921 US 21921


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-20

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