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Open, Classified

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

FDA Recall Z-2101-2025 · Posted 2025-07-09

Recall StatusOpen, Classified
Product CodeOWB
Date Initiated2025-05-27
Product Quantity3 units

Reason for Recall

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

Firm 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].

Root Cause

Under Investigation by firm

Distribution Pattern

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

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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