Spacelabs Medical Incorporated Ultraview Universal Clinical Workstation System Model 90385. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Ultraview Universal Clinical Workstation System Model 90385.
Brand
Spacelabs Medical Incorporated
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Universal Ultraview Clinical Workstation Model 90385 base versions with Revision M or earlier. This recall involves certain units within the serial number range SN: 385-000337 to SN: 385-111440. The firm indicated that not all serial numbers within this range are affected by this recall, but only those units with the specified Revision M or earlier base which have not already been updated.
Spacelabs Medical Incorporated is recalling Ultraview Universal Clinical Workstation System Model 90385. due to Weakness of the swivel base for the universal clinical workstation may result in the unit falling from its mounted position endangering users and pat. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Weakness of the swivel base for the universal clinical workstation may result in the unit falling from its mounted position endangering users and patients.
Recommended Action
Per FDA guidance
All US customers were sent a Medical Device Recall letter on 1/7/2005 describing how to examine monitors for the defect and to discontinue use of any suspect unit s until examintaion by a Field Service Engineer . International customers will be notified via email or letter on 1/14/2005. Follow up contact by Customer Support and Global Support is planned for any customer not responding with a FAX-back form.
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 noticeDistribution
As reported by FDA
IN, OR
Page updated: Jan 10, 2026