Mindray DS USA, Inc., dba Datascope Patient Monitoring Panorama Patient Monitoring Network with ambulatory telepacks, and software version 8.5.5, 8.5.6, 8.6.1 or 8.7. Datascope Patient Monitoring Intended for use in a fixed location, in the healthcare facility setting, as a central viewing station. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Panorama Patient Monitoring Network with ambulatory telepacks, and software version 8.5.5, 8.5.6, 8.6.1 or 8.7. Datascope Patient Monitoring Intended for use in a fixed location, in the healthcare facility setting, as a central viewing station.
Brand
Mindray DS USA, Inc., dba Datascope Patient Monitoring
Lot Codes / Batch Numbers
Software version 8.5.5, 8.5.6, 8.6.1, or 8.7.
Products Sold
Software version 8.5.5, 8.5.6, 8.6.1, or 8.7.
Mindray DS USA, Inc., dba Datascope Patient Monitoring is recalling Panorama Patient Monitoring Network with ambulatory telepacks, and software version 8.5.5, 8.5.6, 8. due to Software Anomaly: Software anomaly can occur when the Panorama is attempting to play an audio file, either a physiological or technical alarm sound, . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software Anomaly: Software anomaly can occur when the Panorama is attempting to play an audio file, either a physiological or technical alarm sound, at which time the system software may cause the system to freeze due to an interaction in the alarm system.
Recommended Action
Per FDA guidance
Urgent Product Field Correction letters, dated March 27, 2009, were sent by certified mail, return requested, and signature required. The letters identified the affected product and the problem. It also stated the adverse effect on patients and that customers' Panorama software will be upgraded to a current software revision. A Datascope Service Representative will contact customers to arrange for the software upgrade of the Panorama(s) in their facility. This will be done at no cost to the customer.
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