Medtronic recalls O-arm O2 imaging systems with specific serial numbers due to potential electrical shock during internal component servicing. Affected units may require repair to prevent shock to technicians.
During servicing of certain internal components of the O-Arm O2 Surgical Imaging System, it is possible that the high-power cable connector may come in contact with surrounding metal during the disconnecting/reconnecting process which may result in an electrical short and a shock to the field service technician.
Medtronic is recalling certain O-arm O2 imaging systems that could cause electrical shock to field service technicians during internal component servicing. This is a safety issue for medical professionals who maintain the equipment.
During servicing of internal components, the high-power cable connector may contact surrounding metal, causing an electrical short and shock to the technician. This hazard occurs only during specific maintenance procedures.
Healthcare facilities using the O-arm O2 Imaging System with the listed serial numbers are affected. Field service technicians who work on these systems are at risk during maintenance.
Check if your O-arm O2 Imaging System has a serial number starting with 'C' followed by numbers from the list provided in the recall notice. The system is used for medical imaging in hospitals and clinics.
Do not service the system until the manufacturer has issued a repair or replacement.
The O-arm O2 Imaging System is a mobile x-ray system designed for 2D and 3D imaging in medical procedures for patients weighing 60 lbs or greater with abdominal thickness over 16cm.
Check the serial number against the list of affected units provided in the recall notice, which starts with 'C' followed by specific numbers.
The recall does not specify a remedy, but the manufacturer will likely provide a repair or replacement for affected units.
We’ve drafted a message you can send Medtronic to request your refund or repair — edit it as you like.
Subject: Recall Z-0927-2018 — Medtronic Medtronic Hello, I own a Medtronic that is covered by recall Z-0927-2018 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.
