Rhytec Inc. Portrait PSR3 System, an electro-surgical device used in dermatological applications Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Portrait PSR3 System, an electro-surgical device used in dermatological applications
Brand
Rhytec Inc.
Lot Codes / Batch Numbers
Software versions prior to Version V2.0A
Products Sold
Software versions prior to Version V2.0A
Rhytec Inc. is recalling Portrait PSR3 System, an electro-surgical device used in dermatological applications due to Inadequate Directions for Use: Software Upgrade to set maximum energy level at 2.5 Hz. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Inadequate Directions for Use: Software Upgrade to set maximum energy level at 2.5 Hz
Recommended Action
Per FDA guidance
Rhytec notified users by letter dated 10/2/06 of the software upgrade. A service representative will perform the update.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026