WebAug 13, 2024 · 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, 2024–January 1, 2024. Baxter Healthcare initiated the recall on July 7, 2024. Baxter Healthcare is recalling SIGMA Spectrum Infusion Pumps with Master Drug Library (Version 8) and Spectrum IQ Infusion Systems with Dose IQ Safety Software (Version 9) due to the risk of not alarming for repeated upstream occlusion events. After an upstream occlusion alarm, failure to fully resolve any … See more On December 29, 2024, Baxter sent an Urgent Safety Communication to all affected customers with the following instructions: 1. Clinicians may continue to use Spectrum V8 and … See more The SIGMA Spectrum Infusion Pump with Master Drug Library (Version 8) and Spectrum IQ Infusion System with Dose IQ Safety Software … See more
Spectrum Mobile™ Return Policy
WebSpectrum IQ Infusion Systems with Dose IQ Safety Software Due to Unplanned Shutdown Issues The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Products • Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) WebAug 13, 2024 · If the correct configuration isn’t showing up on the pump, they should report it to their pharmacy department and proceed to manually program the pump in basic mode. The recall comes a little... barilla werbung
Baxter Warns of Spectrum Infusion Pump Problems
WebProduct Description: Spectrum IQ Infusion System with Dose IQ Unique Device Identifier: Safety Software 00085412610900 Serial Number: All Manufacturing Date: June 29, 2024 - Present Release Date: Dec. 6, 2024 - Present Released Quantity (Units): 175,028 Check the full recall details on fda.gov Source: FDA WebMar 16, 2024 · Baxter International has issued a Class I recall—the most serious type of recall—for its its Spectrum V8 and Spectrum IQ infusion pumps. This recall arrives on the heels of a recent urgent safety communication regarding the upstream occlusion alarms of the devices.. The U.S. FDA says use of the baxter infusion pump devices may cause … WebAug 24, 2024 · Summary Company Announcement Date: August 24, 2024 FDA Publish Date: August 24, 2024 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Multiple Connectivity Errors Company Name: Baxter International Inc. Brand Name: Brand Name(s) Spectrum IQ Product Description: Product Description Infusion … suzuki 600 gsx r 2020 price