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Home » Early Version Software Issues Cause Class I Recall for Medfusion 4000 Syringe Pump
Early Version Software Issues Cause Class I Recall for Medfusion 4000 Syringe Pump
The FDA has deemed Smiths Medical’s recall of its Medfusion model 4000 syringe pump as Class I for software issues that can make the pump fail and delay or interrupt therapy or fail to deliver therapy according to the programmed setting.