Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging functions. Update to software version 3.1.7 resolves the issue.
Software anomalies were reported to affect the following system functionalities: startup and shutdown, system and network communication, motion control, image acquisition and output, dose reporting, and logs generation. Software version 3.1.7 will be installed on all 2nd edition imaging systems.
Medtronic is recalling O-arm 1000 2nd Edition Imaging Systems due to software anomalies that could affect startup, shutdown, communication, motion control, and imaging functions. This recall is important because outdated software may cause system failures during medical procedures.
Software anomalies in the system could cause issues with startup and shutdown processes, communication between components, motion control, image acquisition, and dose reporting. These problems might lead to incomplete or inaccurate imaging during medical procedures.
Healthcare facilities using the O-arm 1000 2nd Edition Imaging System with model number Bl70000027 are affected. Medical professionals and patients using this system for imaging procedures are at risk of potential system failures.
The recalled product is the O-arm 1000 2nd Edition Imaging System with model number Bl70000027. It was sold with all serial numbers as specified in the recall notice.
Install software version 3.1.7 to resolve the reported software anomalies.
The model number is Bl70000027.
Software version 3.1.7 will be installed on all 2nd edition imaging systems.
The recall states software anomalies could affect system functions, but no specific injury risks are mentioned.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0271-2019 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0271-2019 from Medtronic. 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.
