Spacelabs Medical Inc. Ultraview Universal Clinical Workstation Model 90385. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ultraview Universal Clinical Workstation Model 90385.
Brand
Spacelabs Medical Inc.
Lot Codes / Batch Numbers
serial numbers 385-3xxxxx or higher
Products Sold
serial numbers 385-3xxxxx or higher
Spacelabs Medical Inc. is recalling Ultraview Universal Clinical Workstation Model 90385. due to Potential for telemetry channels to drop off display.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Potential for telemetry channels to drop off display.
Recommended Action
Per FDA guidance
For all US customers, a Medical Device Correction letter was mailed on May 7, 2004 via courier instructing their customers to insure all monitored patients are displayed. The letter also instructed customers to move the printer to another central monitor as well as having a Field Service Engineer install new software when it becomes available. This letter was also mailed to international customers on May 14, 2004.
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