Smiths Medical ASD Inc. recalls Medfusion Syringe Pump Model 3500, Software Version V6.0. I
Recalled Product
Medfusion Syringe Pump Model 3500, Software Version V6.0. Infusion pump.
Hazard / Issue
Inaccurate delivery can occur following an interrupted Bolus or Loading dose, if a specific sequence of events occurs.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model Numbers: 3500-0600-00, 3500-0600-01, 3500-0600-249, 3500-0600-50, 3500-0600-51, 3500-0600-82. Software Version V6.0
View official government recall
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your state.
Looking for safe alternatives?
Browse certified-safe products in this category on Amazon →
Get the next US recall alert before it hits the news.
Free. Weekly digest or instant alerts. Unsubscribe anytime.
CAN-SPAM compliant · No spam · Unsubscribe anytime