Overview of recall records associated with Medtronic Navigation, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 48, Class I: 7.
Medtronic Navigation, Inc. announces a voluntary field action for the Medtronic Navigation StealthStation Software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
Medtronic Navigation, Inc. announces a voluntary field action for the Medtronic Navigation StealthStation Software applications affected by Neurologica BodyTom/CereTom floor-based scanners.
Potential for the Visualase Cooled Laser Applicator System (VCLAS) catheters to melt during procedures.
Medtronic Navigation is recalling the Biotex Adapter Kit because it was commercially distributed by BioTex without a cleared premarket [510(k)] from FDA.
Screws holding the detector panel in as a result the detector panel could make contact with other parts with in the 0-arm 02 Imaging System, causing noise and vibration when being…
Specific use conditions can increase the possibility of a screwdriver tip deforming or breaking during surgery.
Specific use conditions can increase the possibility of a screwdriver tip deforming or breaking during surgery.
This page summarizes recall records in which the official source identifies Medtronic Navigation, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
