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BAKRI TAMPONADE BALLOON CATHETER Adverse Event — Malfunction (MDR 1820334-2020-00876)

BAKRI TAMPONADE BALLOON CATHETER Adverse Event — Malfunction (MDR 1820334-2020-00876) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BAKRI TAMPONADE BALLOON CATHETER; Generic name: OQY INTRAUTERINE BALLOON; Manufacturer: COOK INC.

DeviceBAKRI TAMPONADE BALLOON CATHETER
Generic nameOQY INTRAUTERINE BALLOON
ManufacturerCOOK INC
Report number1820334-2020-00876
Event typeMalfunction
Product problemY
Date received2020-04-28
Report sourceDISTRIBUTOR, FOREIGN, OTHER, USE
NarrativeTHIS REPORT INCLUDES INFORMATION KNOWN AT THIS TIME. A FOLLOW UP REPORT WILL BE SUBMITTED SHOULD ADDITIONAL RELEVANT INFORMATION BECOME AVAILABLE.
SourceopenFDA MAUDE (device adverse events)

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