FDAJune 26, 2020device

Medfusion Syringe Pump Model 3500, Software Version V6.0. Infusion pump.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Inaccurate delivery can occur following an interrupted Bolus or Loading dose, if a specific sequence of events occurs.

What to do

FDA enforcement status: Ongoing

Brands named

smiths medical asdsmithssmiths medical

UPCs

35000600249

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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