FDA Recall Open, Classified

O-arm O2 Imaging System. Mobile X-Ray System.

Recall: Z-2101-2025 · Initiated May 27, 2025

Recall

Recall Number
Z-2101-2025
Event Number
97045
Firm
Medtronic Navigation, Inc.-Boxborough
FEI Number
3004785967
Product Code
OWB
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
May 27, 2025
Posted
July 9, 2025
Address
200 Beaver Brook Road, Boxborough, MA, 01719

Description

O-arm O2 Imaging System. Mobile X-Ray System.

Reason

A mechanical component that supports the O2 gantry to the support structure in affected devices may have been damaged during manufacture.

Action

An URGENT: MEDICAL DEVICE CORRECTION notice dated 5/27/25 was mailed to consignees. In the notice consignees are instructed to discontinue use of affected systems until it can be serviced by Medtronic personnel; a copy of the recall notification is to be posted with the system until the issue has been resolved. A Medtronic Field Service Engineer will contact consignees to schedule a visit to inspect affected systems and implement any corrections needed. Consignees are to complete and return the provided Customer Confirmation Form and forward the recall notification to all users and facilities to which product was further distributed. Consignees with any questions can contact Technical Services for help by phone at 1-888-826-5603 or by email at [email protected].

Distribution

US Nationwide distribution in the states of IN, MN, MS.

Quantity

3 units