Smiths Medical Medfusion Recall

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Smiths Medical Recalls Certain Medfusion Pumps for …

https://www.fda.gov/medical-devices/medical-device-recalls/smiths-medical-recalls-certain-medfusion-3500-and-4000-syringe-infusion-pumps-software-issues-may

Smiths Medical is recalling Medfusion 3500 and 4000 Syringe Infusion Pumps for eight software malfunctions that affect different serial numbers and software versions. These malfunctions may cause serious harm or death to patients from under- or over-infusion, or delays in the delivery of critical medications t… See more

Medfusion 3500 and 4000 Syringe Pumps by Smiths …

https://www.asahq.org/advocacy-and-asapac/fda-and-washington-alerts/fda-alerts/2021/01/medfusion-3500-and-4000-syringe-pumps-by-smiths-medical-class-i-recall

ISSUE: Smiths Medical is recalling specific software versions of the Medfusion 3500 and 4000 Syringe Pumps because of a software error that may lead to over-delivery or under …

UPDATED URGENT MEDICAL DEVICE RECALL NOTICE …

https://www.smiths-medical.com/-/media/M/Smiths-medical_com/Files/Alerts/recall_notice_medfusion_3500_4000_inappropriate_bolus_loading_dose_delivery.pdf

Smiths Medical continues to investigate this matter and will follow up with affected customers. Adverse events or quality problems experienced with the use of this product …

Medfusion ® 3500 and 4000 Alerts and Notices - Smiths Medical

https://www.smiths-medical.com/customer-support/alerts-and-notices/medfusion-3500-and-4000-inappropriate-bolus-or-loading-dose-delivery

Smiths Medical Product Alerts And Notices Smiths Medical Product Alerts And Notices Medfusion ® 3500 and 4000 Alerts and Notices Operators Manual Insert Read More …

Smiths Medical Recalls Medfusion 3500 and 4000 …

https://voice.ons.org/news-and-views/smiths-medical-recalls-medfusion-3500-and-4000-syringe-infusion-pumps-for-software

July 21, 2022 On July 20, 2022, the U.S. Food and Drug Administration (FDA) reported Smiths Medical’s recall of its Medfusion 3500 and 4000 syringe infusion pumps …

Class 1 Device Recall Medfusion - Food and Drug …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=182138

Smiths Medical ASD Inc. 6000 Nathan Ln N Minneapolis MN 55442-1690: For Additional Information Contact: Dave Halverson 763-383-3072 Manufacturer …

Class 2 Device Recall Medfusion 3500 V5 Syringe …

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=107698

Class 2 Device Recall Medfusion 3500 V5 Syringe Pumps. Smiths Medical, Medfusion¿ 3500 Syringe Pumps, Software version 5.0.0, Rx Only. These …

Smiths Medical Recalls Medfusion 3500 and 4000 Syringe …

https://www.goldenberglaw.com/blog/2022/august/smiths-medical-recalls-medfusion-3500-and-4000-s/

In April 2022, Smiths Medical recalled Medfusion 3500 and 4000 Syringe Infusion Pumps due to software malfunctions that can impact infusion delivery. 118,055 …

Smiths Medical warned by FDA for multiple violations

https://www.raps.org/news-and-articles/news-articles/2021/11/smiths-medical-warned-for-multiple-violations-in-f

The company makes blood warmers and infusion pumps. The warning letter was issued on 1 October and posted on 23 November. It follows a recent recall of the …

Smiths Medical Recalls Medfusion 3500 and …

https://www.brockgoetzmann.com/smiths-medical-recalls-medfusion-3500-and-4000-syringe-pumps/

Smiths Medical is recalling versions of the Medfusion 2500 and 4000 Syring Pumps due to software errors. These errors may lead to over-delivery or under …

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