Medical device Adverse Event — Malfunction (MDR 8010042-2008-00012)

Name: Medical device Adverse Event — Malfunction (MDR 8010042-2008-00012)
Creator: DeviceEvents

Medical device Adverse Event — Malfunction (MDR 8010042-2008-00012) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Report number: 8010042-2008-00012; Event type: Malfunction; Date received: 2008-02-01.

Report number	8010042-2008-00012
Event type	Malfunction
Date received	2008-02-01
Report source	Foreign, Health Professional, User facility, Company representation
Narrative	MAQUET INC. SUBMITS THIS REPORT ON BEHLAF OF THE DEVICE MFG FACILITY. MAQUET CRITICAL CARE AB PROVIDES PRODUCT FAILURE INVESTIGATION, ANALYSIS AND RESOLUTION FOR THE DEVICE DESCRIBED IN THIS REPORT.
Source	openFDA MAUDE (device adverse events)

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