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CONNECT SFTY SCREW SPIKE NS Adverse Event — Malfunction (MDR 1282497-2020-09044)

CONNECT SFTY SCREW SPIKE NS Adverse Event — Malfunction (MDR 1282497-2020-09044) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CONNECT SFTY SCREW SPIKE NS; Generic name: PUMP, INFUSION, ENTERAL; Manufacturer: COVIDIEN.

DeviceCONNECT SFTY SCREW SPIKE NS
Generic namePUMP, INFUSION, ENTERAL
ManufacturerCOVIDIEN
Report number1282497-2020-09044
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, CONSUM
NarrativeTHE INCIDENT SAMPLE HAS BEEN REQUESTED BUT TO DATE HAS NOT BEEN RECEIVED FOR EVALUATION. IF THE SAMPLE IS RECEIVED, OR IF ADDITIONAL INFORMATION PERTINENT TO THE INCIDENT IS OBTAINED A FOLLOW-UP REPORT WILL BE SUBMITTED. AS PART OF OUR MANUFACTURING PROCESS, ALL DEVICE HISTORY RECORDS ARE REVIEWED AND APPROVED BY QUALITY, PRIOR TO RELEASE OF PRODUCT.
SourceopenFDA MAUDE (device adverse events)

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