Dec 01 2021 Recent Recalls involving devices. 2021 12 01 Arrow Trerotola Over The Wire PTD Kit Percutaneous Thrombolytic Device 7R by Teleflex Incorporated Class I RecallDue to Inner Lumen Detaching From the Device’s Basket 2021 11 12 Updates on Philips Respironics CPAP BiPAP and Ventilator Recall 2021 11 10 Custom Convenience Kits by Aligned
Oct 07 2016 The Medicines and Healthcare Products Regulatory Agency MHRA has advised that certain lots of the Accu Chek Insight Tender infusion set are being recalled due to a potential issue of the patch not being sticky enough.These are lots of the Accu Chek Insight Tender infusion set used with the Accu Chek Insight diabetes therapy system. This may
Medtronic MiniMed Sure T infusion sets Recall for Product Correction 23rd June 2015. Potential for interruption of insulin delivery and/or infection due to needle breaking during use Medtronic after consultation with the TGA TGA Ref# RC 2015 RN 00506 1 is initiating a voluntary Recall for Product Correction for the above mentioned
BETHLEHEM PAAugust 28 2019B. Braun Medical Inc. B.Braun initiated a voluntary recall of one lot of Infusomat Space Volumetric Infusion Pump Administration Sets Catalog Number 363032 Lot Number . The recalled administration sets are used to deliver parenteral fluids. B.Braun identified through customer complaints the potential of the infusion
Jan 22 2022 The voluntary recall was issued over concerns that products may contain benzene a known carcinogen. It involves multiple lots of 32 P G dry shampoo or conditioner spray products in a range of sizes. Procter Gamble issued a voluntary recall after some reports indicated that benzene was been found in certain P G aerosolized spray products.
8mL or 3mL reservoirs can be used in the MiniMed 640G Custom made for Medtronic MiniMed 640G MiniMed Paradigm 5 and 7 Series Insulin Pumps Can be used with all MiniMed infusion sets If your Total Daily Dose of Insulin Basal insulin plus typical meal time Bolus insulin is less than 48 units you may want to consider using the 1.
Sep 11 2017 Medtronic an Ireland based medical device firm with an a location in Littleton announced Monday a recall of infusion sets with all models of the company s insulin pumps.
FDA RecallICU Medical Infusion Sets We are writing to inform you that effective immediately the FDA has published notice of a voluntary recall issued by ICU Medical Inc. of certain lots of Plum and Sapphire Microbore Infusion Sets with inline filters due to the potential for small amounts of fluid leaking o.. Read More 2019 10 03
Sep 11 2017 Sept 11 Reuters Medtronic Plc Medtronic announces voluntary recall of diabetes infusion sets Medtronic determined a component vent membrane in recalled infusion sets may be susceptible
0 ml 300 unit Infusion Sets Medtronic Diabetes provides a variety of infusion sets to fit your needs. The FCA involves Medtronic updating their Instructions for Use IFU to. Paradigm Reservoirs have also been designed with a great deal of
Jul 13 2009 The Medtronic Paradigm recall involves one lot of Quick set infusion sets which are disposable plastic tubes used to infuse a diabetes patient from the Medtronic insulin pump. They are usually
Jun 28 2021 This indicates that the Medtronic Extended infusion set delivers insulin successfully throughout the seven day wear of the infusion set. Medtronic issues voluntary recall for TurboHawk 6Fr
Apr 27 2020 On Sept. 16 2019 the company initiated a voluntary recall to notify customers that certain lots of BodyGuard Microset infusion sets when used with the BodyGuard infusion pump may under
Alert on voluntary recall and corrective action by Defibtech on semi automatic external defibrillators 15 Apr 2011 Recall of microbial contaminated protective wipes and adhesive removers 02 Mar 2011 Safety alert on ACCU CHEK FlexLink Plus infusion sets 11 Feb 2011 Safety concern on Fraxel re store Dual Laser System 27 Jan 2011
Sep 13 2017 Medtronic announced Sept. 11 that it has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps. The recall is for a certain discontinued component in these infusion sets and does not include insulin pumps or glucose Diabetes
Apr 06 2006 April 2006Disetronic Medical Systems Inc Disetronic of Fishers Ind. announced a voluntary nationwide recall of all ACCU CHEK Ultraflex Infusion Sets because of a potential that tubing could fully or partially separate at the luer lock tubing connection. In the event that a full or partial separation occurs it is possible that insulin
Sep 10 2017 MEDTRONIC ANNOUNCES VOLUNTARY RECALL OF DIABETES INFUSION SETS BRAMPTONSeptember 10 2017Medtronic Canada a subsidiary of Medtronic plc NYSE MDT announced today that Medtronic has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin
Sep 13 2017 Medtronic recalls some MiniMed insulin infusion devices Premium Medtronic recalling MiniMed insulin infusion devices is likely to have an impact on India often called the diabetes capital of the
Apr 08 2006 This recall applies to all ACCU CHEK Ultraflex infusion sets. Patients using any standard luer lock insulin pump may also be using these ACCU CHEK Ultraflex infusion sets. Disetronic is advising customers to check their infusion sets at the luer lock tubing connection at least every 3 hours and before bedtime.
Nov 22 2019 Becton Dickinson NYSE BDX said today it has updated two voluntary recalls of certain Alaris infusion pump modules and infusion sets used with those modules. The FDA has designated both recalls as Class I as the agency has received reports of several serious injuries associated with the recalled devices.
B. Braun Medical Inc. B. Braun initiated a voluntary recall of twenty two 22 lots of Blood Administration Sets. The recalled blood administration sets are used to administer blood from a container to a patient s vascular system through an IV catheter inserted into a
Medtronic Urgent Recall of MiniMed Insulin Infusion Sets. Washington DC Medtronic in conjunction with the US Food and Drug Administration
Sep 11 2017 Medtronic has initiated a worldwide voluntary recall of specific lots of MiniMed infusion sets used with all models of Medtronic insulin pumps. The company said it has determined that the vent
Sep 13 2017 Medtronic is telling patients that certain lots of its infusion sets for its insulin pumps are being recalled as part of a voluntary effort.. The problematic infusion sets which patients can identify by checking REF and LOT numbers on the available site have a vent membrane that may be more likely to get blocked possibly leading to too high levels of
Jul 15 2013 The Medtronic MiniMed Paradigm Insulin Infusion Set recall was announced by the U.S. Food and Drug Administration on June 7 due to an issue where fluids may come in contact with the tubing