Medtronic recalls O-arm 1000 2nd Edition Imaging Systems with software anomalies affecting startup, shutdown, communication, motion control, and imaging. Update to software version 3.1.7 to resolve issues.
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, image acquisition, and dose reporting. Updating to software version 3.1.7 resolves these issues.
Software anomalies could cause problems with the system's startup and shutdown, communication, motion control, image acquisition, and dose reporting. This might lead to inconsistent imaging results or inaccurate patient data during procedures.
Healthcare professionals using the O-arm 1000 2nd Edition Imaging System for medical procedures. Patients undergoing imaging with this system may be affected if the software issues impact their treatment.
The product has the model number Bl70000027100R and is part of the O-arm 1000 2nd Edition Imaging System. It was sold with the serial number starting with Bl70000027100R.
Install software version 3.1.7 to fix the reported software anomalies affecting system functions.
Software anomalies were reported that could affect startup, shutdown, communication, motion control, image acquisition, and dose reporting in the O-arm 1000 2nd Edition Imaging System.
Your system is affected if it has the model number Bl70000027100R and is part of the O-arm 1000 2nd Edition Imaging System.
Install software version 3.1.7 to resolve the software anomalies reported in the system.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0274-2019 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0274-2019 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.
