AORTIC ARCH CANNULAE, OPTIFLOW AORTIC ARCH CANNULA A282-70A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-01-09 for AORTIC ARCH CANNULAE, OPTIFLOW AORTIC ARCH CANNULA A282-70A manufactured by Sorin Group Italia Srl.

MAUDE Entry Details

Report Number9680841-2020-00003
MDR Report Key9568216
Report SourceHEALTH PROFESSIONAL
Date Received2020-01-09
Date of Report2019-12-10
Date Mfgr Received2020-03-27
Device Manufacturer Date2019-11-11
Date Added to Maude2020-01-09
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 ContactENRICO GRECO
Manufacturer Street14401 W 65TH WAY
Manufacturer CityARVADA CO 80004
Manufacturer CountryUS
Manufacturer Postal80004
Manufacturer G1SORIN GROUP ITALIA SRL
Manufacturer StreetSTRADA STATALE 12 NORD, 86
Manufacturer CityMIRANDOLA 41037
Manufacturer CountryIT
Manufacturer Postal Code41037
Single Use3
Remedial ActionOT
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAORTIC ARCH CANNULAE, OPTIFLOW AORTIC ARCH CANNULA
Generic NameCATETHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
Product CodeDWF
Date Received2020-01-09
Returned To Mfg2020-01-16
Model NumberA282-70A
Catalog NumberA282-70A
Lot Number1911110040
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSORIN GROUP ITALIA SRL
Manufacturer AddressSTRADA STATALE 12 NORD, 86 MIRANDOLA, MODENA US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-09

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