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Medtronic Navigation, Inc.-Boxborough recalls

Every recall we track for Medtronic Navigation, Inc.-Boxborough — 2 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them.

2recalls

Recalls per year, by danger level

2 recalls since 2017.

2017: 0 recalls20172018: 0 recalls20182019: 0 recalls20192020: 0 recalls20202021: 0 recalls20212022: 0 recalls20222023: 0 recalls20232024: 0 recalls20242025: 1 recall — 1 use caution120252026 (to date): 1 recall — 1 lower risk12026to date

All FDA recall records for Medtronic Navigation, Inc.-Boxborough since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.

Recalls per year for Medtronic Navigation, Inc.-Boxborough, by danger level
YearStop using nowUse cautionLower riskNot yet ratedTotal
201700000
201800000
201900000
202000000
202100000
202200000
202300000
202400000
202501001
2026 (to date)00101

What to do if you have a recalled Medtronic Navigation, Inc.-Boxborough product

  1. Match the model, catalog or lot number on your device to the recall.
  2. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
  3. Report problems to FDA MedWatch.

See this week’s new recalls.

All Medtronic Navigation, Inc.-Boxborough recalls

2 shown

Medtronic Navigation, Inc.-Boxborough recall questions

How many recalls has Medtronic Navigation, Inc.-Boxborough had?

2 recalls from Medtronic Navigation, Inc.-Boxborough are on record with U.S. safety agencies, from 2025–2026.

What is the most recent Medtronic Navigation, Inc.-Boxborough recall?

Medtronic Navigation, Inc.-Boxborough recalls Medtronic O-arm O2 Imaging System. Model Number: BI70002000., dated May 19, 2026. Every Medtronic Navigation, Inc.-Boxborough recall is listed on this page, newest first.

What should I do if I have a recalled Medtronic Navigation, Inc.-Boxborough product?

Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.

How do I get alerts for new Medtronic Navigation, Inc.-Boxborough recalls?

Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.