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 units currently out in the market.
Products Sold
All units currently out in the market.
Datascope Corp is recalling Panorama Patient Monitoring Network. Cardiac Arrhythmia Monitor. due to Upon the new release of software, the firm started receiving reports of unexpected system failures in the database subsystem related to virtual memory. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Upon the new release of software, the firm started receiving reports of unexpected system failures in the database subsystem related to virtual memory pages.
Recommended Action
Per FDA guidance
The firm sent a field correction communications to all customers via certified mail on 6/10/2005. A Datascope Service Representative will conduct and document this 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