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HIGH FLOW NASAL CANNULA WITH HEATED CHAMBER FISHER AND PAYKEL Reports 1998-2010
Medical Device Brand Name: FISHER PAYKEL
Medical Device Generic Name: HIGH FLOW NASAL CANNULA WITH HEATED CHAMBER
Medical Device Manufacturer Name:FISHER AND PAYKEL


HIGH FLOW NASAL CANNULA WITH HEATED CHAMBER FISHER AND PAYKEL Report # 1047111
HEATED CHAMBER SHATTERED DUE TO BEING OVER-PRESSURED. THE HUMIDIFIER HEATER WAS OFF AT THE TIME OF THE INCIDENT. NO WATER WAS IN THE CHAMBER, JUST OXYGEN FLOW. PATIENT CIRCUIT WAS ATTACHED TO PATIENT WITHOUT PRESSURE RELIEF VALVE. NO HARM TO THE PATIENT. AFTER THE INVESTIGATION WITH THE EQUIPMENT, FISHER & PAYKEL REPRESENTATIVE RECOMMENDED TO ADD THE PRESSURE RELIEF VALVE TO THE SYSTEM. THE POLICY & PROCEDURE HAS BEEN CHANGED AND THE PRESSURE RELIEF VALVE HAS BEEN ADDED TO THE EQUIPMENT FOR PATIENT SAFETY. SEE SCANNED PAGES.


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Source: Manufacturer and User Facility Device Experience Database - (MAUDE). MAUDE data represents reports of adverse events involving medical devices. The data consists of voluntary reports since June 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August 1996. MAUDE may not include reports made according to exemptions, variances, or alternative reporting requirements granted under 21 CFR 803.19. MAUDE is scheduled to be updated quarterly and the search page reflects the date of the most recent update. MAUDE data is not intended to be used either to evaluate rates of adverse events or to compare adverse event occurrence rates across devices. Please be aware that reports regarding device trade names may have been submitted under different manufacturer names. Searches only retrieve records that contain the search term(s) provided by the requester. The data is updated on a quarterly basis. DISCLAIMER: Section 21 CFR 803.16 states that "A report or other information submitted by a reporting entity under this part, and any release by FDA of that report or information, does not necessarily reflect a conclusion by the party submitting the report or by FDA that the report or information constitutes an admission that the device, or the reporting entity or its employees, caused or contributed to the reportable event. The reporting entity need not admit and may deny that the report or information submitted under this part constitutes an admission that the device, the party submitting the report, or employees thereof, caused or contributed to a reportable event." In addition, some firms have submitted their own additional disclaimer statements. A file of those disclaimers will be placed on the web shortly.
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