FDA recall Z-2449-2023

Medtronic Navigation, Inc.-Littleton · Class II · device

Product

The O-arm O2 Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and pediatric patients weighing 60 lbs. or greater and having an abdominal thickness greater than 16 cm and is intended to be used where a physician benefits from 2D and 3D information of anatomic structures and objects with high x-ray attenuation such as bony anatomy and metallic objects.

Reason for recall

Ground cable installed incorrectly.

Distribution

Worldwide - US Nationwide distribution in the states of CA, CO, FL, IA, IL, IN, KY, MI, MO, NC, NV, OH, TN, UT, VA, & WA. The countries of Canada, Ireland, Poland, Russian Federation, Switzerland, & Viet Nam.

Key facts

Status
Ongoing
Initiation date
2023-07-25
Report date
2023-08-30
Voluntary/Mandated
Voluntary: Firm initiated
Location
Littleton, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2449-2023