Omega Medical Imaging recalls elevating monitor suspension systems (part 1000-0085) manufactured 2012-2019 due to risk of lower boom detachment. Affected units may require inspection or replacement.
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.
Omega Medical Imaging is recalling elevating monitor suspension systems from 2012 to 2019 because a lower boom can detach from the pivot mechanism. This could cause the boom to become restrained by the safety cable, potentially leading to injury if the monitor falls.
The actuator can separate from the pivot mechanism on the lower monitor boom system column. When this happens, the lower boom may detach and become restrained by the installed safety cable, which could lead to injury if the monitor falls.
Medical professionals using elevating monitor suspension systems with part number 1000-0085 are most at risk. Units manufactured between October 2012 and July 2019 are affected.
Check for part number 1000-0085 on the elevating monitor suspension system. Units were manufactured between October 2012 and July 2019.
Inspect the lower monitor boom system column for any signs of actuator separation from the pivot mechanism.
This recall affects elevating monitor suspension systems with part number 1000-0085 manufactured between October 2012 and July 2019.
Check if your unit has part number 1000-0085 and was manufactured between October 2012 and July 2019. If so, inspect the lower boom system column for actuator separation.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send Omega Medical Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-0160-2024 — Omega Medical Imaging Omega Medical Imaging Hello, I own a Omega Medical Imaging that is covered by recall Z-0160-2024 from Omega Medical Imaging. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
