MAUDE Adverse Event Report: VARIAN EHR SOFTWARE

Device Problem Computer Operating System Problem (2898)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 05/31/2016

Event Type  malfunction  

Event Description

E-prescriptions were sent using aria ehr software produced by (b)(4).They were never received by (b)(6) pharmacy on (b)(6).Ehr vendor informed, but insists that prescriptions were sent.Pharmacy insists they never received them.

• Brand Name: EHR SOFTWARE
• Type of Device: EHR SOFTWARE
• Manufacturer (Section D): VARIAN
• MDR Report Key: 5705315
• MDR Text Key: 46780402
• Report Number: MW5062700
• Device Sequence Number: 1
• Product Code: LLZ
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 06/05/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/05/2016
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Age: 78 YR
• Patient Weight: 64