Recall of Medtronic Xomed NIM Vital Console 4.0 (P/N: NIM4CM01) with software version 1.3.2 due to a software anomaly. Affected units include specific model numbers and lot numbers.
Software anomaly was identified.
Medtronic Xomed is recalling NIM Vital Console 4.0 devices with software version 1.3.2 because of a software anomaly. This recall affects specific model numbers and lot numbers listed in the notice. Users should check their device details to see if they are affected.
The recall states a software anomaly was identified, but the specific hazard mechanism is not described in the notice. Without details on how this anomaly could cause harm, the risk level cannot be determined.
Users of the NIM Vital Console 4.0 device with software version 1.3.2 and specific model numbers and lot numbers listed in the recall notice are affected. Medical device users are most at risk.
Check if your device has model number NIM4CM01 and software version 1.3.2. Affected units include specific lot numbers listed in the recall notice.
Identify your device's model number and software version to see if it matches NIM4CM01 with version 1.3.2.
The recall states a software anomaly was identified, but the specific issue details are not provided in the notice.
Check if your device has model number NIM4CM01 and software version 1.3.2, and if it matches the listed lot numbers in the recall notice.
The recall does not specify any remedy steps, so users should check the official notice for further instructions.
We’ve drafted a message you can send Medtronic Xomed to request your refund or repair — edit it as you like.
Subject: Recall Z-1223-2022 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-1223-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
