In September 2015, CareFusion issued emergency Class 1 recalls for its Alaris Syringe pumps. The pump was supposedly programmed to administer scheduled medical infusions to patients. As per official reports, due to a software code error (leading to a malfunction), the infusion pump could (or might already) have wrongly administered the scheduled medication, putting patient lives at risk. In response, the company issued recalls, regulators got involved, and the reputation damage was immediate.