https://plainrecords.com/brand/remington-medical/New recalls of Remington Medical from FDA, CPSC and NHTSA records.en-ushttps://plainrecords.com/recall/device/z-0487-2024/https://plainrecords.com/recall/device/z-0487-2024/Wed, 13 Dec 2023 00:00:00 +0000There is an error with the "Use by Date" and "Date of Manufacturer" on the box label.https://plainrecords.com/recall/device/z-0771-2023/https://plainrecords.com/recall/device/z-0771-2023/Wed, 04 Jan 2023 00:00:00 +0000The stylet is longer than specified on the labelhttps://plainrecords.com/recall/device/z-1441-2014/https://plainrecords.com/recall/device/z-1441-2014/Wed, 16 Apr 2014 00:00:00 +0000Remington Medical discovered an error on the FL-601-97 IFU; part number IFU-RM-0154. Specifically, the polarity for the black chuck in the picture is wrong. It shows (+), but should show (-).https://plainrecords.com/recall/device/z-0028-2013/https://plainrecords.com/recall/device/z-0028-2013/Wed, 17 Oct 2012 00:00:00 +0000Sterility of the product may be compromised.https://plainrecords.com/recall/device/z-2405-2011/https://plainrecords.com/recall/device/z-2405-2011/Thu, 02 Jun 2011 00:00:00 +0000There have been complaints of the Drainage Bags leaking from the outlet and the inlet port.https://plainrecords.com/recall/device/z-1573-2011/https://plainrecords.com/recall/device/z-1573-2011/Mon, 07 Mar 2011 00:00:00 +0000There is a potential for the needle hubs to break during use.https://plainrecords.com/recall/device/z-2223-2010/https://plainrecords.com/recall/device/z-2223-2010/Fri, 13 Aug 2010 00:00:00 +0000The Safe Connect component may separate from the cable, causing the cable to become unplugged from the EPG.https://plainrecords.com/recall/device/z-1935-2009/https://plainrecords.com/recall/device/z-1935-2009/Sun, 20 Sep 2009 00:00:00 +0000Two unsealed pouches were identified after product release, compromising product sterility.https://plainrecords.com/recall/device/z-1417-2009/https://plainrecords.com/recall/device/z-1417-2009/Tue, 26 May 2009 00:00:00 +0000Incorrect needle (Franseen Needle, FNM-1806) was packaged as a Chiba Needle Marked.https://plainrecords.com/recall/device/z-0058-2008/https://plainrecords.com/recall/device/z-0058-2008/Tue, 23 Oct 2007 00:00:00 +0000Sterility, inadequate -- Pathway may not be sterile as labeled.https://plainrecords.com/recall/device/z-0673-2007/https://plainrecords.com/recall/device/z-0673-2007/Thu, 29 Mar 2007 00:00:00 +0000Pouches were not sealed prior to sterilization.https://plainrecords.com/recall/device/z-0124-06/https://plainrecords.com/recall/device/z-0124-06/Thu, 03 Nov 2005 00:00:00 +0000The vector selector has an electrical design flaw which prevents RV pacing.https://plainrecords.com/recall/device/z-0065-06/https://plainrecords.com/recall/device/z-0065-06/Fri, 21 Oct 2005 00:00:00 +0000The Tear-Away introducer sheath in the Disposable Tear-Away Vascular Introducer kits may exhibit cracked hubs/handles and/or improper peeling of the sheath during use.https://plainrecords.com/recall/device/z-0697-05/https://plainrecords.com/recall/device/z-0697-05/Fri, 08 Apr 2005 00:00:00 +0000The stylet hub detaches from the stylet needle.