https://plainrecords.com/brand/newport-medical-instruments/New recalls of Newport Medical Instruments from FDA, CPSC and NHTSA records.en-ushttps://plainrecords.com/recall/device/z-1874-2017/https://plainrecords.com/recall/device/z-1874-2017/Wed, 10 May 2017 00:00:00 +0000Medtronic is issuing a voluntary field corrective action for all its Newport" HT70 and Newport" HT70 Plus ventilators because they may shutdown spontaneously during normal operation without an accompanying alarm.https://plainrecords.com/recall/device/z-1171-2013/https://plainrecords.com/recall/device/z-1171-2013/Wed, 08 May 2013 00:00:00 +0000Newport Medical Instruments is conducting a voluntary recall on certain Newport Medical Instruments HT70 and HT70 Plus ventilator Power Pac batteries due to customer reports of Newport HT70 and HT70 Plus ventilators alarming and going to internal backup battery sooner than expected while the ventilator is being operated on Power Pac battery.https://plainrecords.com/recall/device/z-2250-2012/https://plainrecords.com/recall/device/z-2250-2012/Wed, 12 Sep 2012 00:00:00 +0000May emit a continuous high priority alarm and the ventilator may stop ventilating, due to a component failure on the control board.https://plainrecords.com/recall/device/z-2468-2011/https://plainrecords.com/recall/device/z-2468-2011/Wed, 08 Jun 2011 00:00:00 +0000Cregarding e360 ventilators that were shipped with a different software version from what the customers ordered.https://plainrecords.com/recall/device/z-2406-2011/https://plainrecords.com/recall/device/z-2406-2011/Thu, 02 Jun 2011 00:00:00 +0000The recall was initiated because Newport Medical has confirmed a limited number of power cords recently received from their supplier, Glob-Tek, have a slightly oversized plug connector which prevents the cord from locking into place. These cords are fully functional as supplied. However, the cord can be easily disconnected. If the cord is disconnected, the HT70 will alert the user with a power dihttps://plainrecords.com/recall/device/z-2384-2011/https://plainrecords.com/recall/device/z-2384-2011/Fri, 27 May 2011 00:00:00 +0000The recall was initiated because Newport Medical has confirmed that the HT50 Dual Pac Ventilator is not compatiable with the external battery pack (p/n BAT3300A) supplied with the previous single battery ventilator. The Dual Pac system has a slightly higher amperage draw than the single battery and as a result can cause the fuse in the external battery pack to blow making the battery inoperable.https://plainrecords.com/recall/device/z-2382-2011/https://plainrecords.com/recall/device/z-2382-2011/Thu, 26 May 2011 00:00:00 +0000The recall was initiated because Newport Medical has confirmed that the Newport HT50 hard shell Emergency Preparedness (EP) Storage Cases must be relabeled to caution users to follow current labeling guidelines for charging the battery for 8 hours but not longer than 24 hours at any one time.https://plainrecords.com/recall/device/z-2295-2011/https://plainrecords.com/recall/device/z-2295-2011/Thu, 26 May 2011 00:00:00 +0000The recall was initiated because Newport Medical Instruments confirmed that the Newport HT50 ventilators that were shipped in December 2008 were without the label on the top of the ventilator that reminds users to keep HT50 ventilators plugged into an external power supply whenever possible to preserve the longterm capacity of the battery.https://plainrecords.com/recall/device/z-1617-2010/https://plainrecords.com/recall/device/z-1617-2010/Wed, 19 May 2010 00:00:00 +0000The recall was initiated due to a recent increase in complaints related to the early failure of a low pressure transducer which is on Printed Circuit Board (PCB) 2104A in the Newport e360 ventilator. Ventilators manufactured between September and December 2009 are affected by this field correction. All affected ventilators require the replacement of the PCB2104A board to avoid early failure of thttps://plainrecords.com/recall/device/z-2029-2009/https://plainrecords.com/recall/device/z-2029-2009/Fri, 04 Sep 2009 00:00:00 +0000In December 2008, Newport initiated a field correction to upgrade e360 ventilators with software versions 3.0 or higher to software version 3.3. As a result of this upgrade, some customers experienced unexpected device alert alarms. Newport's investigation into these complaints confirmed that the 3.3 software responds too quickly to certain situations, giving a false device alert. Newport conduhttps://plainrecords.com/recall/device/z-1192-2007/https://plainrecords.com/recall/device/z-1192-2007/Wed, 19 Sep 2007 00:00:00 +0000Battery Life: With use over time, the internal battery begins losing its ability to hold a charge resulting in shortened ventilator operation time. Specifically, Newport has received a number of reports concerning the internal battery not lasting as long as expected followed by ventilator shut down with less advance warning than when the battery was new.https://plainrecords.com/recall/device/z-1375-05/https://plainrecords.com/recall/device/z-1375-05/Wed, 17 Aug 2005 00:00:00 +0000Lack of alarm prior to shutdown.