The software product mentioned in this medwatch report may not be, by definition, a medical device; however, cerner has chosen to file this medwatch report in order to voluntarily notify the fda of a malfunction associated with this software product.The company's filing of this medwatch report does not signify cerner's belief or understanding that medical device reports are required to be filed for products such as cerner's powerorders and plans, nor are these products currently actively regulated by the fda.This report documents information related to an issue identified with functionality included in cerner's millennium powerorders and plans.This issue involves cerner millennium powerorders and plans and affects users that utilize powerplans to place clinical orders within the emr.When the user creates an order for a future date and time, the system may incorrectly update the order's start date and time to the current date and time.As a result, a patient may receive a treatment earlier than intended.Cerner has not received communication on any adverse patient events as a result of this issue.
|