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Open, Classified

Orthofix NorthStar OCT Navigation Surgical Technique Guide, and instruments: Navigation Driver, REF: PC2-400012; Navigation Straight Bone Probe, REF: PC2-400013; Navigation, 3.5mm Drill, REF: PC2-400135; Navigation, 4.0mm Drill, REF: PC2-400140; Navigation, 4.5mm Drill, PC2-400145; Navigation, 5.5mm Drill, REF: PC2-400155; Navigation, 3.5mm Tap, REF: PC2-400235; Navigation, 4.0mm Tap, REF: PC2-400240; Navigation, 4.5mm Tap, REF: PC2-400245; Navigation, 4.5mm Dual Lead Tap, REF: PC2-400345; Navigation, 5.5mm Dual Lead Tap, REF: PC2-400355

FDA Recall Z-0937-2026 · Posted 2025-12-17

Recall StatusOpen, Classified
Product CodeOLO
Date Initiated2025-11-17
Product Quantity310

Reason for Recall

The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic s Solera and Medtronic s Infinity system toolcards as compatible with the NorthStar OCT Navigation Instruments. However, the NorthStar OCT Navigation Instruments are compatible for use with Medtronic s Solera toolcards only.

Firm Action

On 10/27/2025, device correction notices were emailed to customers who were informed of the following: The NorthStar OCT Navigation Surgical Technique Guide (STG) incorrectly identified both Medtronic's Solera and Medtronics Infinity system StealthStation tool cards as compatible with the NorthStar OCT Navigation Instruments; however, the NorthStar OCT Navigation Instruments are indicated for use with Medtronic's Solera tool cards only. 1) Discontinue use of Medtronic's Infinity tool cards with NorthStar OCT Navigation instruments. 2) Discard affected version of the Surgical Technique Guide 3) This notice should be shared within your organization and forwarded to any organization where affected Instruments and guide is utilized. 4) Review updated Surgical Technique Guide D0003926 Revision DA. This notice should be shared within your organization and forwarded to any organization where affected instruments are utilized. Any product complaints should be reported to Orthofix at [email protected]

Root Cause

Labeling design

Distribution Pattern

US: CT, TX, NV, CO, CA, WA, NJ, OR, IN, MI, FL, PA, IL, VA, AL, RI, MO, AZ, MS, SC, UT, NY, OK, SD. OUS: Australia, Mexico, Chile

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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