Z-0686-2007

Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software

Name: Z-0686-2007 Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
Creator: Aspyra, Inc.
Published: 2007-01-31
License: https://open.fda.gov/license/

Aspyra, LLC. / initiated 2007-01-31 / Terminated

FDA source

Aspyra, Inc. began a recall of Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software on 2007-01-31. The reason FDA records is "Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0686-2007
Status: Terminated
Initiated: 2007-01-31
Posted: 2007-03-31
Terminated: 2011-07-22
Recalling firm: Aspyra, LLC.
Product: Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
Product code: NXS
Reason for recall: Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient.
FDA root 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
Product codes and lots: Version 2.1

Product code NXS

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)