Aspyra, Inc. Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
Brand
Aspyra, Inc.
Lot Codes / Batch Numbers
Version 2.1
Products Sold
Version 2.1
Aspyra, Inc. is recalling Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software due to Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026