Class 2 Device Recall CyberMED Version 2.1 Pharmacy SoftwareAspyra

• Date Initiated by Firm: January 31, 2007
• Date Posted: March 31, 2007
• Recall Status: Terminated on July 22, 2011
• Recall Number: Z-0686-2007
• Recall Event ID: 37277
• Product Classification: Medication Administration - Product Code NXS
• Product: Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
• Code Information: Version 2.1
• FEI Number: 3001452787
• Recalling Firm/ Manufacturer: Aspyra, Inc.; 26115 Mureau Rd; Calabasas CA 91302-3177
• For Additional Information Contact: Martin D. Sargent; 800-437-9000 Ext. 2107
• Manufacturer Reason for Recall: Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient.
• FDA Determined Cause: Other
• Action: Current customers were mailed a Recall Letter January 31,2007 explaining the issue and informing the customers of an upcoming CyberMED Version 2.1 maintenance software release to correct the potential issue. A fax-back Acknowledgement of Receipt form was sent with the Recall Letter.
• Quantity in Commerce: 10
• Distribution: Nationwide to: CA, GA, IN, MI, MN, MS, NC, ND, & OK

¹ A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
² Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
³ For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 �7.55.