Medtronic Xomed recalls NIM Vital Patient Interface 4.0 with software version 1.3.2 due to a software anomaly. Affected units have specific model numbers and lot numbers listed in the recall notice.
Software anomaly was identified.
Medtronic Xomed is recalling NIM Vital Patient Interface 4.0 devices with software version 1.3.2 because of a software anomaly. This recall matters because the software issue could potentially cause problems with device operation, though the exact risk is not specified in the recall notice.
The recall states a software anomaly was identified, but does not specify the exact hazard mechanism or how it could cause harm. Without more details, it's unclear what risks this software issue poses to device users.
Patients using the NIM Vital Patient Interface 4.0 with software version 1.3.2 are likely affected. Those with the specific model numbers and lot numbers listed in the recall notice are at the highest risk.
Check if your device has model number NIM4CPB1 and software version 1.3.2. Affected units include specific lot numbers listed in the recall notice.
Verify your device's model number and software version to see if it matches the recalled units.
The recall states a software anomaly was identified but does not specify the exact hazard or risk level.
The recall does not provide a remedy, so no specific action is required beyond checking if your device is affected.
Check if your device has model number NIM4CPB1 and software version 1.3.2, and if it matches the listed lot numbers 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-1224-2022 — Medtronic Xomed Medtronic Xomed Hello, I own a Medtronic Xomed that is covered by recall Z-1224-2022 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.
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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.
