Datascope Corp Panorama Patient Monitoring Network, Cardiac Arrhythmia Monitor. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Panorama Patient Monitoring Network, Cardiac Arrhythmia Monitor.
Brand
Datascope Corp
Lot Codes / Batch Numbers
All Panorama Central Station containing software versions 8.1.6 - 8.2
Products Sold
All Panorama Central Station containing software versions 8.1.6 - 8.2
Datascope Corp is recalling Panorama Patient Monitoring Network, Cardiac Arrhythmia Monitor. due to Software anomaly that affects the Panorama Telepack where if communications are lost during standby, certain alarms which appear set could be actually. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Software anomaly that affects the Panorama Telepack where if communications are lost during standby, certain alarms which appear set could be actually off.
Recommended Action
Per FDA guidance
Datascope sent letters to the distributors and end users on 12/7/2005. This communication states that a Datascope Service Representative will conduct and document the corrective action during a visit 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