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,health report with the FDA on 2020-02-06 for TITAN STABILIZER ATTACHMENT T401231 N/A manufactured by Terumo Cardiovascular Systems Corporation.

Event Text Entries

[188527292] 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


[188527293] The user facility reported to terumo cardiovascular that during cardiopulmonary bypass, while using the titan stabilizer, the right metal wishbone part of the footplate rubbed a hole in the heart. A hemostatic agent was used to stop the bleeding. There was approximately 100 ml of blood loss, there was minimal delay, the product was not changed out, the surgery was completed successfully.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1124841-2020-00021
MDR Report Key9679645
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-02-06
Date of Report2020-03-13
Date of Event2020-01-16
Date Mfgr Received2020-03-10
Device Manufacturer Date2018-09-10
Date Added to Maude2020-02-06
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTITAN STABILIZER ATTACHMENT
Generic NameUNIVERSAL STABILIZER ARM
Product CodeMWS
Date Received2020-02-06
Returned To Mfg2020-01-30
Model NumberT401231
Catalog NumberN/A
Lot Number00107
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
101. Other; 2. Required No Informationntervention 2020-02-06

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