Medtronic O-arm O2 Imaging System recall — FDA Z-2451-2026
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
Overview of recall records associated with Medtronic Navigation, Inc.-Boxborough, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.
This page summarizes recall records in which the official source identifies Medtronic Navigation, Inc.-Boxborough 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.