baxter spectrum iq recall

  • Medical Device Correction Baxter Sigma Spectrum

    Operators may continue to use the Spectrum infusion pumps until the correction is completed The software upgrade for Spectrum IQ is available and will be implemented upon next service or a local Baxter service representative will contact you facility to schedule the software upgrade.

  • Technical Service Portal

    Global Technical Services Baxter is committed to making it easier to get the support you need through online solutions and service plans Hospital service departments are required to support a complex network of medical devices and ensure they are always available for clinical use which puts great demands and pressure on the biomed.

  • Baxter 2020 Sustainability Accounting Standards Board Index

    included the following Baxter medical device product Sigma Spectrum Infusion Pumps V6 V8 and IQ Baxter issued an Urgent Device Correction to reinforce important safety information regarding cleaning practices and communicated that Spectrum Instructions for Use would be

  • Best Selling Large Volume Infusion Pumps in the United

    In February 2020 the FDA issued a Class I recall on all Alaris pumps in the US which is expected to cause BD to lose market share to other competitors mentioned below 2 Spectrum IQ Large Volume Infusion Pump Company Baxter Pump Size Small Units Sold/ASP Request your MedSKU Sample

  • Spectrum IQ

    Baxter Smart IV Pump SOMETHING RATHER BIG FOR A SMALL INFUSION PUMP Spectrum IQ Infusion System revolutionizes the traditional idea of an integrated smart pump Building on the Spectrum platform s industry leading drug library compliance and ease of use Spectrum IQ infusion system now fully integrates with your EMR adding another layer of safety to your

  • Public Health Messages

    Spectrum IQ Infusion System with Dose IQ Safety Software All Customers with additional questions can contact their Baxter sales representative or Baxter Technical Assistance at 800 356 3454 choose option 1 Monday through Friday

  • Baxter Announces U.S

    May 14 2018  Deerfield Ill.2018 05 14 Baxter International Inc NYSE BAX a leader in innovative technology for medication delivery today announced the U.S Food and Drug Administration FDA clearance of the Spectrum IQ Infusion System with Dose IQ Safety Software The Spectrum IQ system is the first of its kind designed specifically for bi

  • More Problems For Software Used In Baxter Spectrum IQ

    Aug 26 2021  The US Food and Drug Administration said on 12 August that it gave its highest risk classification class I to a recall of Dose IQ Safety Software used with the Spectrum IQ pumps In that case the software was recalled by Baxter Healthcare because a defect could lead to mismatched drug information in drug libraries created using version 9

  • Spectrum IQ Infusion System with Dose IQ Safety Software

    Nov 26 2020  Medical Device Recall Subcategory Medical Device Hazard classification Type II Source of recall Health Canada Issue 2020 12 10 Reason Affected products Affected Products Spectrum IQ Infusion System with Dose IQ Safety Software Reason Baxter Healthcare Corporation 1 Baxter Parkway Deerfield 60015 Illinois

  • Baxter Issues Urgent Medical Device Correction for All

    Baxter International Inc announced today it has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps to reinforce important safety information when customers implement changes to their network configuration and server systems Baxter previously communicated this informatio Source link

  • Baxter SIGMA Spectrum Infusion Pumps with Master Drug

    Dec 02 2020  Recall of Baxter SIGMA Spectrum Infusion Pumps with Master Drug Library Versions 6 and 8 and Spectrum IQ Infusion Systems with Dose IQ Safety Software by Baxter Healthcare due to unplanned shutdown.

  • Baxter Healthcare Recalls Dose IQ Software Version 9.0.x

    Aug 12 2021  Baxter Healthcare Recalls Dose IQ Software Version 9.0.x Used with Spectrum IQ Infusion Pumps for Software Defect That May Improperly Configure Drug and Fluid Delivery Medication Safety Healthcare Professional Aug 12 Written By

  • Baxter Issues Urgent Device Correction to ..

    Oct 28 2020  Company Announcement Baxter International Inc announced today it has issued an Urgent Device Correction to reinforce important safety information regarding cleaning practices of all Spectrum infusion pumps distributed in the United States Canada and the Caribbean as deviations from the specified cleaning methods may impair infusion pump functionality and

  • Alerts by year

    Dec 23 2020  Recall of Baxter SIGMA Spectrum Infusion Pumps with Master Drug Library Versions 6 and 8 and Spectrum IQ Infusion Systems with Dose IQ Safety Software by Baxter Healthcare due to Read More Recalls Dec 02 2020 Happy Ducts Compress by

  • Baxter Healthcare Recalls Dose IQ Software Version 9.0.x

    Feb 01 2018  The recall affects 61 devices of the Dose IQ Safety Software used with the Spectrum IQ Infusion System with software version 9.0.x and product code 35723V091.The software was distributed from February 1 2018 January 1 2019 Baxter Healthcare initiated the recall on July 7 2021.

  • BAX

    fda says baxter healthcare recalls dose iq software version 9.0.x used with spectrum iq infusion pumps aug 12 reuters u.s fda fdabaxter healthcare recalls dose

  • Baxter Issues Urgent Medical Device Correction for All

    Baxter International Inc announced today it has issued an Urgent Medical Device Correction for all Spectrum IQ infusion pumps to reinforce important safety information when customers implement changes to their network configuration and server systems Baxter previously communicated this informatio

  • BAXTER INTERNATIONAL INC BAX Interactive Stock Chart

    The FDA issued a Class I recall the most serious kind of recall for Baxter International Inc s NYSE BAX Dose IQ safety software used with Spectrum IQ Infusion System.

  • Baxter Healthcare Recalls Dose IQ Software Version 9.0.x

    Aug 12 2021  Baxter Healthcare is recalling the Dose IQ Safety Software used with the Spectrum IQ Infusion System A software defect may lead to mismatched drug information in drug libraries created using version 9.0.x of the computer based software.

  • Drug Information Center Highlights of FDA Activities 12/1

    Baxter SIGMA Spectrum Infusion Pumps and Spectrum IQ Infusion Systems Recall Unplanned Shutdown Issues 12/1/20 Baxter Healthcare recalled the Baxter Healthcare Sigma Spectrum Infusion Pumps with Master Drug Library V6 V8 and the Baxter Spectrum IQ Infusion Systems with Dose IQ Safety Software V9 because improper cleaning of the

  • Baxter Healthcare Recalls Baxter SIGMA Spectrum Infusion

    Dec 01 2020  Reason for Recall Baxter Healthcare is recalling the Baxter Healthcare Sigma Spectrum Infusion Pumps with Master Drug Library V6 V8 and the Baxter Spectrum IQ Infusion Systems with Dose IQ Safety Software V9 because improper cleaning of the devices may lead to residue build up or corrosion on the device.

  • Provider Newsflash FDA RECALL

    We are writing to inform you that effective immediately the FDA has issued a Class I recall of Baxter Healthcare’s SIGMA Spectrum Infusion Pumps with Master Drug Library Versions 6 8 and Spectrum IQ Infusion Systems with Dose IQ Safety Software V9 due to the potential for unplanned shutdown issues.

  • Class 2 Device Recall SPECTRUM IQ INFUSION SYSTEM WITH

    Sep 18 2018  SPECTRUM IQ INFUSION SYSTEM WITH DOSE IQ SAFETY SOFTWARE Code Information UDI All Serial Numbers distributed prior to 07/09/2018 Recalling Firm Manufacturer Baxter Healthcare Corporation 711 Park Ave Medina NY 14103 1036 For Additional Information Contact Center for One Baxter 800 422 9837

  • Baxter International Inc

    Find the latest Baxter International Inc BAX stock quote history news and other vital information to help you with your stock trading and investing.

  • Baxter Healthcare Recalls Dose IQ Software Version 9.0.x

    Aug 12 2021  Baxter Healthcare is recalling the Dose IQ Safety Software used with the Spectrum IQ Infusion System A software defect may lead to mismatched drug information in drug libraries created using

  • Infusion Pump Recall Archives

    Aug 31 2021  Baxter Spectrum IQ Infusion Pump Recall Issued Due To Software Defects August 31 2021 By Russell Maas Software problems have led to a recall of Baxter Spectrum IQ infusion pumps which may

  • FDA Class I Recall of Baxter s Dose IQ Infusion Pump Software

    Aug 18 2021  Baxter has reported that a defect was found in its Dose IQ software can transmit incorrect drug dosing information to its Spectrum IQ infusion pumps If this occurs the patient could be at risk for injury or severe adverse events including death.

  • BAX shares Baxter International Inc stock performance

    Sep 01 2021  On August 13 2021 FDA FDA issued a Class I recall the most serious kind of recall for Baxter International Inc’s BAX Dose IQ safety software used with Spectrum IQ Infusion System The Dose IQ safety software allows care providers to create a drug library of pre programmed dosing information for specific medications delivered into a

  • Baxter Issues Urgent Medical Device Correction for All

    Aug 24 2021  Baxter Issues Urgent Medical Device Correction for All Spectrum IQ Infusion Pumps to Reinforce Important Safety Information Regarding Best Practices for Customer Initiated IT Network Updates August 24 2021 in Recalls from FDA by Heather Davis

  • Baxter Recalls Dose IQ Software 9.0.x Used With Infusion

    Aug 13 2021  The FDA issued a Class I recall the most serious kind of recall for Baxter International Inc’s NYSE BAX Dose IQ safety software used with Spectrum IQ Infusion System. The Dose IQ safety software allows care providers to create a drug library of pre programmed dosing information for specific medications delivered into a person’s body in

  • 24x7 Magazine

    24x7 Magazine August 13 at 12 55 PM Baxter has initiated a safety recall for its Spectrum Dose IQ Safety Software due to a potentially life threatening defect in which incorrect drug dosing information could be transmitted to the company’s Spectrum IQ Infusion System The potential for patient harm is so serious in fact that the U

  • Global Intravenous Infusion Pumps Market By Type By

    Oct 26 2021  May 2018 Baxter International received the clearance of the Spectrum IQ Infusion System with Dose IQ Safety Software from the U.S Food and Drug Administration FDA .

  • Recalls by year

    Recall of Baxter SIGMA Spectrum Infusion Pumps with Master Drug Library Versions 6 and 8 and Spectrum IQ Infusion Systems with Dose IQ Safety Software by Baxter Healthcare due to Read More Recalls Dec 02 2020 Happy Ducts Compress by WishGarden Herbs.

  • Spectrum IQ Infusion System with Dose IQ Safety Software

    Sep 04 2020  Spectrum IQ Infusion System with Dose IQ Safety Software Reason This is a follow up communication to the urgent Medical Device Safety Alert Baxter previously issued on April 7 2020 to reinforce important safety information regarding cleaning practices of spectrum infusion pumps.

  • Recalls Archives

    Oct 28 2021  Baxter NYSE BAX this week issued an urgent medical device correction for all of its Spectrum IQ infusion pumps Earlier this month FDA designated a recall of Baxter’s Dose IQ safety software program as Class I its most serious level Baxter designed the Dose IQ as a standalone computer based software program that allows care providers to

  • Spectrum IQ Infusion System with Dose IQ Safety Software

    Jun 10 2021  Spectrum IQ Infusion System with Dose IQ Safety Software 2021 06 10 Report a Concern Starting date June 10 2021 Posting date June 23 2021 Type of communication Medical Device Recall Subcategory