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28MM DIA COCR MOD HD -3MM NK Adverse Event — Injury (MDR 0001825034-2020-01807)

28MM DIA COCR MOD HD -3MM NK Adverse Event — Injury (MDR 0001825034-2020-01807) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: 28MM DIA COCR MOD HD -3MM NK; Generic name: PROSTHESIS, HIP; Manufacturer: ZIMMER BIOMET, INC..

Device28MM DIA COCR MOD HD -3MM NK
Generic namePROSTHESIS, HIP
ManufacturerZIMMER BIOMET, INC.
Report number0001825034-2020-01807
Event typeInjury
Product problemY
Date received2020-04-28
Report sourceCOMPANY REPRESENTATIVE, DISTRI
NarrativeNO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
SourceopenFDA MAUDE (device adverse events)

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