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Terminated

Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software

FDA Recall Z-0686-2007 · Posted 2007-03-31

Recalling FirmAspyra, Inc.
Recall StatusTerminated
Product CodeNXS
Date Initiated2007-01-31
Date Terminated2011-07-22
Product Quantity10

Reason for Recall

Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient.

Firm 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.

Root Cause

Other

Distribution Pattern

Nationwide to: CA, GA, IN, MI, MN, MS, NC, ND, & OK

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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