Recall of Device Recall CyberMED Version 2.1 Pharmacy SoftwareAspyra

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Aspyra, Inc..

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    37277
  • Event Risk Class
    Class 2
  • Event Number
    Z-0686-2007
  • Event Initiated Date
    2007-01-31
  • Event Date Posted
    2007-03-31
  • Event Status
    Terminated
  • Event Country
  • Event Terminated Date
    2011-07-22
  • Event Source
    USFDA
  • Event Source URL
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Medication Administration - Product Code NXS
  • Reason
    Medications prescribed for one patient were printed on the medication administration record (mar) of another patient.
  • 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.

Device

  • Model / Serial
    Version 2.1
  • Distribution
    Nationwide to: CA, GA, IN, MI, MN, MS, NC, ND, & OK
  • Product Description
    Aspyra, Inc. CyberMED Version 2.1 Pharmacy Software
  • Manufacturer

Manufacturer

  • Manufacturer Address
    Aspyra, Inc., 26115 Mureau Rd, Calabasas CA 91302-3177
  • Source
    USFDA