A Drug & Medical Device Recall And/Or Safety Alert Has Been Issued: Smiths Medical Medfusion Model 4000 Syringe Infusion Pump: Class I Recall – System Errors May Cause Device Shutdown. According to the Food & Drug Administration FDA’s MedWatch:
Delay or interruption of infusion therapy could result in serious injury and/or death.
For more information on the drug or medical device recall or safety alert, read the Food & Drug Administration’s FDA’s drug or medical device recall or safety alert: Smiths Medical Medfusion Model 4000 Syringe Infusion Pump: Class I Recall – System Errors May Cause Device Shutdown.
To report an adverse reaction, problem or other issue with a drug or medical device, submit a drug or medical device complaint to the government at fda.gov or MedWatch.
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