Arthrex® AR-7905Recalls & reported problems
Arthrex, Inc. · Anterior Cannula, ZoneNavigator · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867300460), received between Feb 24, 2026 and Feb 24, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Failure to Advance” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Failure to Advance2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 24, 2026Failure to Advance
ON 7TH FEB 2026, IT WAS REPORTED BY AN ARTHREX'S EMPLOYEE VIA AN EMAIL THAT FOR 2 UNITS OF AR-7905, ZONENAVIGATOR¿ SYSTEM CANNULA - ANTERIOR, VE5, THE MENISCUS NEEDLE COULD NOT GO THROUGH BOTH THE CANNULA (REFER TO VIDEO). THIS WAS DETECTED DURING A MEDIAL MENISCUS REPAIR (BUCKET HANDLE TEAR) ON (B)(6) 2026. THE PROCEDURE WAS COMPLETED SUCCESSFULLY BY USING AR-7910R INSTEAD. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24432875 ↗MalfunctionFeb 24, 2026Failure to Advance
ON 7TH FEB 2026, IT WAS REPORTED BY AN ARTHREX'S EMPLOYEE VIA AN EMAIL THAT FOR 2 UNITS OF AR-7905, ZONENAVIGATOR¿ SYSTEM CANNULA - ANTERIOR, VE5, THE MENISCUS NEEDLE COULD NOT GO THROUGH BOTH THE CANNULA (REFER TO VIDEO). THIS WAS DETECTED DURING A MEDIAL MENISCUS REPAIR (BUCKET HANDLE TEAR) ON (B)(6) 2026. THE PROCEDURE WAS COMPLETED SUCCESSFULLY BY USING AR-7910R INSTEAD. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24432874 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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