FDA Medical Device Recalls (openFDA)
Aspyra, Inc.: Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
- Recall number
- Z-0686-2007
- Recalling firm
- Aspyra, Inc.
- Product
- Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
- Status
- Terminated
- Initiated
- 2007-01-31
- Posted
- 2007-03-31
- Terminated
- 2011-07-22
- Reason
- Medications prescribed for one patient were printed on the Medication Administration Record (MAR) of another patient.
- 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
- 10
- Distribution
- Nationwide to: CA, GA, IN, MI, MN, MS, NC, ND, & OK
- Lot, serial or model codes
- Version 2.1
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- NXS
- Firm FEI
- 3001452787
- Firm city
- Calabasas
- Firm state
- CA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28