# FDA device recall: Medtronic O-arm O2 Imaging System. Model Number: BI70002000.

> recall · VERIFIED · 2026-05-19

Firm: Medtronic Navigation, Inc.-Boxborough · Class II · Potential for image artifacts caused by an anomaly in the O-arm O2 Imaging System s detector panel firmware.

- Company: Medtronic Navigation, Inc.-Boxborough
- Sector: medtech
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.