Medtronic Xomed recalls specific IPC software versions due to potential M5 Microdebrider rotating at higher speed than set during surgical procedures. Affected units include model 1898072 with listed lot numbers.
During internal testing execution of the next generation of Integrated Power Console (IPC) prototype it was noted that the M5 Microdebrider was rotating at a higher speed than the set value in the cosole.
Medtronic Xomed is recalling software version 2.7.3.0 for their IPC system. This update could cause the M5 Microdebrider to spin faster than intended during surgery, potentially leading to tissue damage. Affected units have specific lot numbers listed in the recall notice.
During internal testing, the M5 Microdebrider was observed rotating at a higher speed than the value set in the IPC console. This could cause the device to cut tissue faster than intended during surgical procedures, potentially leading to unintended tissue damage.
Surgical professionals using the Medtronic Xomed IPC system with the affected software version are most at risk. Patients undergoing procedures with this specific software version could experience unintended tissue damage.
Check if your IPC system has software version 2.7.3.0 (model 1898072). Affected units include specific lot numbers listed in the recall notice, such as 0217355465 and others.
Verify your IPC system's software version by checking the device settings or documentation.
Reach out to Medtronic Xomed directly for assistance with the recall and to confirm if your unit is affected.
During internal testing, the M5 Microdebrider was observed rotating at a higher speed than the value set in the IPC console, which could cause unintended tissue damage during surgery.
Software version 2.7.3.0 for model 1898072 IPC system.
Check if your IPC system has software version 2.7.3.0 and if your lot number matches the list provided in the recall notice.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-2673-2020 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-2673-2020 from Medtronic Xomed. 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.
