Mobius Imaging recalls detachable 10in pendant upgrade components for AIRO CT X-ray systems due to missing "Safe Hand Position Warning" label. Affected units may pose safety risks during use.
AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.
Mobius Imaging is recalling detachable 10-inch pendant upgrade components for their AIRO CT X-ray systems because these parts lack the required "Safe Hand Position Warning" label. This missing label could lead to improper hand positioning during use, potentially causing injury.
The pendant upgrade components lack the "Safe Hand Position Warning" label, which is critical for ensuring proper hand positioning during X-ray procedures. Without this label, healthcare workers might not be aware of the correct positioning, increasing the risk of injury to themselves or patients.
Healthcare professionals using AIRO CT X-ray systems with the specific pendant upgrade components are most at risk. Patients and staff may be affected if the components are used without the safety label.
Check for the part number MI-70-0128 on the pendant upgrade component. The serial numbers listed in the recall include 2232206183 through 2323513413 and other specific numbers. These components were sold with AIRO CT X-ray systems.
Inspect the pendant upgrade component for the "Safe Hand Position Warning" label. If missing, it is part of the recall.
The pendant upgrade components lack the required "Safe Hand Position Warning" label, which is critical for ensuring proper hand positioning during X-ray procedures.
Check if the component has the "Safe Hand Position Warning" label. If missing, it is part of the recall and you should stop using it until a replacement is obtained.
Yes, the affected serial numbers include 2232206183, 2232206193, 2232206203, and other specific numbers listed in the recall notice.
We’ve drafted a message you can send Mobius Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-1041-2026 — Mobius Imaging Mobius Imaging Hello, I own a Mobius Imaging that is covered by recall Z-1041-2026 from Mobius 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.
