ANGEL CPRP PROCESSING SET US ABS-10063

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,distri report with the FDA on 2018-10-01 for ANGEL CPRP PROCESSING SET US ABS-10063 manufactured by Arthrex, Inc..

Event Text Entries

[122193195] The contribution of the device to the reported event could not be determined as the device was not returned for evaluation. The device was reported to have been discarded. The cause of the event could not be determined from the information available and without device evaluation.
Patient Sequence No: 1, Text Type: N, H10


[122193196] It was reported that during a prp procedure, the tubing by the light sensor began to leak. The blood spilled out and was cleaned and the kit was properly disposed of. A second kit was opened and used to complete a second draw and the procedure was completed.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1220246-2018-00676
MDR Report Key7922634
Report SourceCOMPANY REPRESENTATIVE,DISTRI
Date Received2018-10-01
Date of Report2018-10-01
Date of Event2018-09-10
Date Mfgr Received2018-09-10
Device Manufacturer Date2018-02-22
Date Added to Maude2018-10-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactVIK BAJNATH
Manufacturer Phone8009337001
Manufacturer G1ARTHREX, INC.
Manufacturer Street1370 CREEKSIDE BOULEVARD
Manufacturer CityNAPLES FL 341081945
Manufacturer CountryUS
Manufacturer Postal Code341081945
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameANGEL CPRP PROCESSING SET US
Generic NamePLATELET AND PLASMA SEPARATOR FOR BONE GRAFT HANDLING
Product CodeORG
Date Received2018-10-01
Model NumberANGEL CPRP PROCESSING SET US
Catalog NumberABS-10063
Lot Number2017110044
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerARTHREX, INC.
Manufacturer Address1370 CREEKSIDE BOULEVARD NAPLES FL 341081945 US 341081945


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2018-10-01

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