NOT PROVIDED UNKNOWN

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 2020-03-09 for NOT PROVIDED UNKNOWN manufactured by Angiodynamics.

Event Text Entries

[188553230] The reported defective device has yet to be returned to the manufacturer for a device evaluation. The firm is attempting to obtain the device. An investigation into the root cause for product problem is currently in progress. The results of the device evaluation will be sent via a follow up medwatch. Complaint # (b)(4).
Patient Sequence No: 1, Text Type: N, H10


[188553231] A patient of unknown age and gender was receiving continuous renal replacement therapy (crrt) via an angiodynamics dialysis catheter (product name nor number was provided) when it was noted the catheter had a small pinhole in it. It was reported the patient had the catheter removed and replaced as he/she required further dialysis treatments. There was no harm or injury to the patient due to this event. It was reported the defective disposable device is available for return to the manufacturer for evaluation. .
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1319211-2020-00016
MDR Report Key9805800
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2020-03-09
Date of Report2020-03-09
Date of Event2020-01-28
Date Mfgr Received2020-02-17
Date Added to Maude2020-03-09
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 ContactLAW RYAN
Manufacturer Street10 GLENS FALLS TECHNICAL PARK
Manufacturer CityGLENS FALLS, NY
Manufacturer CountryUS
Manufacturer Phone7424488
Manufacturer G1ANGIODYNAMICS
Manufacturer Street10 GLENS FALLS TECHNICAL PARK
Manufacturer CityGLENS FALLS, NY
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameNOT PROVIDED
Generic NameUNKNOWN
Product CodeMSD
Date Received2020-03-09
Catalog NumberUNKNOWN
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerANGIODYNAMICS
Manufacturer Address10 GLENS FALLS TECHNICAL PARK GLENS FALLS, NY US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-09

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