Omega Medical Imaging Monitor Suspension (Omega) - Component Detachment (2023)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085
Brand
Omega Medical Imaging, Inc.
Lot Codes / Batch Numbers
all units manufactured between 10-22-2012 and 07-09-2019
Products Sold
all units manufactured between 10-22-2012 and 07-09-2019
Omega Medical Imaging, Inc. is recalling Omega Medical Imaging Elevating Monitor Suspension, Part Number 1000-0085 due to An actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety ca. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An actuator separated from the pivot mechanism on a lower monitor boom system column and became detached and was restrained by the installed safety cable at one location.
Recommended Action
Per FDA guidance
Omega Medical Imaging issued a Field Safety Advisory Notice to its consignees on 02/28/2023 by email. The notice explained the issue and pledged to evaluate all potentially impacted devices and mitigate the issue to bring the boom systems up to the latest safety design and standard of the newer models approved for field use.
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