Omega Monitor Suspension (Omega Medical) – Boom Detachment (2023)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Omega Medical Imaging Elevating Monitor Suspension Systems, 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 Systems, Part Number 1000-0085 due to An actuator separated from the pivot mechanism on a lower monitor boom system column. The lower boom became detached at the point shown and was restra. 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. The lower boom became detached at the point shown and was restrained by the installed safety cable.
Recommended Action
Per FDA guidance
Omega Medical Imaging issued a Field Safety Advisory Notice to its consignees on 09/08/2023 via email. The notice explained the problem and the risk. The firm will inspect all affected devices to ensure the proper fasteners were installed on the unit.
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
AL, CA, IL, IN, KY, LA, MO, MT, NC, OH, OK
Page updated: Jan 10, 2026