Atlas FDA

Harmonie software versions 5.1 uo to 6.2e : Harmonie-E Long Term Monitoring system (Models HSYS-REC-WD, HSYS-REC-WT; HSY

FDA device recall Z-1080-2013 · posted 2013-04-22 · Terminated

Recall details

Recalling firm
Stellate Systems
Reason for recall
The firm is initiating this recall because the implied or stated indications in their labeling associated with Harmonie software have not yet been cleared by the FDA for sale in the USA.
Action taken
Stellate sent an "DEVICE CORRECTION" letter dated April 6, 2009, to all affected customers. The letter identified the product, the problem and the action needed to be taken by the customer. Customers were instructed to check the product code referenced in the service manual to verify if your system is affected and check in "Help" & "About Harmonie" in the menu to determine the software version on these systems. Stellate will shortly release updates to disable the noted features that were present in your particular version of the Harmonie software and revise labeling and Instructions for Use. All customers in possession of an affected system will be contacted by our Customer Support team to set up an appointment for installation of the updated version. If you have any questions or concerns regarding this notification, please do not hesitate to call our customer support line at 1-888-742-1306.
Root cause
No Marketing Application
Status
Terminated
Product code
GWQ
Quantity affected
2660 Software licenses
Distribution
Worldwide distribution: USA (nationwide) including states of: AL, AR, AZ, CA, CT, DE, FL, HI, IA, IN, IL, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NJ, NY, OH, OR, PA, RI, SC, TX, VA, VT, WI, WV, an
Date initiated
2009-04-06
Date posted
2013-04-22
Date terminated
2013-04-22
Location
Westmount, Canada

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Related 510(k) clearances

RecordFirmDate
HARMONIE SYSTEM (K083577)Stellate Systems2011-08-29
HARMONE-SCHWARZER EEG SYSTEM (K010728)Stellate Systems2001-05-21