The Recall Desk

Manufacturer

Medtronic Xomed, Inc.

26 recalls in our database name Medtronic Xomed, Inc. as the manufacturing or recalling firm.

What the numbers show

Total
26
Critical
0
Severe
6
Most recent
2025-09-03

Of the 26 recalls from Medtronic Xomed, Inc. we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 6 (23%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

26–26 of 26

  • HighFDA (Devices)·Z-2342-2012·2012-09-19

    Medtronic NIM 3.0 Patient Interfaces Recalled for Signal Loss

    Medtronic is recalling NIM 3.0 Patient Interfaces due to a trend of open channel conditions causing signal loss and potential surgical delays.

    Product
    Interfaces subject to recall: Medtronic NIM (Nerve Integrity Monitor) 3.0 Patient Interfaces 8253200 (Response) LABELING: Box Label: REF 8253200 x1***NIM-Response 3.0 Patient Interface***Medtronic Xomed, Inc., 6743 Southpoint Drive North Jacksonville, FL 32216-0980 USA*
    Category
    Medical Device
    Distribution
    Distributed nationwide