Omega Medical Imaging recalls elevating monitor suspension (part 1000-0085) manufactured 2012-2019 due to potential actuator detachment. Affected units may require repair or replacement.
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.
Omega Medical Imaging is recalling elevating monitor suspension units made between October 2012 and July 2019 because an actuator could detach from the pivot mechanism. This poses a risk of the actuator becoming restrained by the safety cable, which could lead to equipment malfunction.
The actuator can separate from the pivot mechanism on the lower monitor boom system column. When this happens, the detached actuator may become restrained by the installed safety cable, potentially causing equipment malfunction.
Medical imaging professionals using the elevating monitor suspension are most at risk. Affected units were manufactured between October 2012 and July 2019.
Check for the part number 1000-0085 on the elevating monitor suspension. Units were manufactured between October 2012 and July 2019.
Inspect the monitor suspension for signs of actuator detachment from the pivot mechanism.
Reach out to Omega Medical Imaging for repair or replacement options.
The part number is 1000-0085.
Units were manufactured between October 2012 and July 2019.
The recall describes a potential actuator detachment that could cause equipment malfunction, but does not specify injury risks.
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-0156-2024 — Omega Medical Imaging Omega Medical Imaging Hello, I own a Omega Medical Imaging that is covered by recall Z-0156-2024 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.
