Mobius Imaging recalls MobiCT-32 AIRO Mobile CT Scanners due to potential injury risks when untrained users move units in reverse. Learn about affected models and safety steps.
Stryker received one report of an injury to an untrained user that occurred while the untrained user was moving an Airo TruCT unit in reverse. The firm will increase visibility of instructions for users to consider when transporting the unit in reverse by providing labels to be affixed onto the AIRO.
Mobius Imaging recalls its MobiCT-32 AIRO Mobile CT Scanners after one report of injury to an untrained user moving the device in reverse. This highlights the need for proper training and clear safety instructions when handling the equipment.
The hazard occurs when untrained users move the AIRO Mobile CT Scanner in reverse without proper awareness, potentially causing injury. The single reported incident involved an untrained person moving the unit in reverse, indicating a risk of accidents due to insufficient guidance.
Untrained users of the MobiCT-32 AIRO Mobile CT Scanners are most at risk when moving the device in reverse. Healthcare facilities using this equipment without proper training should also review safety protocols.
Check for the model MobiCT-32 AIRO Mobile CT Scanner with serial numbers starting with 00869346000200. This product was sold as a mobile computed tomography system.
Check for updated labels on the AIRO unit that provide visibility for reverse movement safety.
The recall reports one injury to an untrained user moving the device in reverse, but no specific details on injury severity or frequency are provided.
Check for the model MobiCT-32 AIRO Mobile CT Scanner with serial numbers starting with 00869346000200.
Review the safety instructions and ensure proper training before moving the device in reverse. Updated labels will be provided for better visibility.
We’ve drafted a message you can send Mobius Imaging to request your refund or repair — edit it as you like.
Subject: Recall Z-0957-2023 — Mobius Imaging Mobius Imaging Hello, I own a Mobius Imaging that is covered by recall Z-0957-2023 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.
