Spectrum iq recall
WebMar 19, 2024 · Recall Status 1: Terminated 3 on July 15, 2024: Recall Number: Z-1487-2024: Recall Event ID: 87568: 510(K)Number: K173084 Product Classification: Pump, infusion - Product Code FRN: Product: Spectrum IQ - Infusion Pump - Product Usage: intended to be used for the controlled administration of fluids. Code Information WebCustomer letters on this page have been mailed directly to customers affected by the specific updates and in some situations include reply forms for customers to return to us. If you have questions or want more information, contact us at: Customer Service Hospital Products & Renal Toll-Free: 1-888-229-0001 (1-224-948-1856)
Spectrum iq recall
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WebAug 31, 2024 · The recall includes the Spectrum IQ Infusion System with Dose IQ Safety Software marked with Product Code: 3570009. The devices were manufactured by Baxter International Inc. of Deerfield ... WebAug 24, 2024 · DEERFIELD, Ill. - 2024-08-24 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.
WebSupport when you need it. Reporting an insurance claim should be easy. With us, it is. Being faced with the unexpected can be a very stressful thing, but we don’t think reporting an … 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 …
WebBaxter is communicating important safety information for Spectrum V8 and Spectrum IQ Infusion Pumps related to potential reduced or non-delivery of medication, in some cases without alerting the user via pump alarm. This may occur as a result of incorrect administration set setup and/or incomplete resolution of upstream occlusion alarms. 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 24, 2024 · Online: By completing and submitting the report online at Online Regular mail or Fax: Download the form from Download form or call 800-332-1088 to request a …
WebDec 2, 2024 · 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. More on the FDA website. baju sadariah dan kebaya encimWebMar 14, 2024 · The recall pertains to Baxter's Spectrum V8 and Spectrum IQ infusion pumps used in clinical settings to deliver controlled amounts of fluids such as pharmaceutical drugs, blood & blood products ... baju sakeraWebClass 2 Device Recall Sigma Spectrum Infusion Pump with Master Drug Library V6, V8, Spectrum IQ with Dose IQ Safety Softwa ... New Search: Back to Search Results : Class 2 Device Recall Sigma Spectrum Infusion Pump with Master Drug Library V6, V8, Spectrum IQ with Dose IQ Safety Softwa: Date Initiated by Firm: January 06, 2024: Create Date ... baju safari adalahBaxter 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 baju safari satpamWebFeb 21, 2024 · The U.S. Food and Drug Administration posed a safety communication late last week, warning about issues with more than 315,000 Baxter Sigma Spectrum V8 and Spectrum IQ infusion pumps, which... aranae setWebDisclaimer Text. Not all products, pricing, and services are available in all areas. Pricing and actual speeds may vary. Internet speeds based on wired connection. baju saiz besar lelakiWebAug 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... baju sakera lengkap