Arthrex® AR-7910LRecalls & reported problems
Arthrex, Inc. · Mid/Post Cannula, Left, ZoneNavigator · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00888867300477), received between May 18, 2021 and Apr 21, 2025 — classified as 3 injuries, 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
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. How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
- Detachment of Device or Device Component1
- Failure to Advance1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Unspecified Infection2
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 21, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
ON 03/31/2025, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS-(B)(4) THAT AN AR-7910L MID/POST CANNULA WAS DISCONNECTED FROM THE PLASTIC GREY PART AND UNABLE TO USE. THIS WAS DISCOVERED DURING THE CASE WITH NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21875681 ↗InjuryDec 27, 2022Failure to Advance
IT WAS REPORTED THAT DURING A MENISCUS SURGERY THE NEEDLE COULD NOT BE ADVANCED AND SO THE SYSTEM INCLUDING THE AR-7905, AR-7910L AND AR-7900 DID NOT WORK. THE SURGERY WAS FINISHED SUCCESSFULLY WITH A DIFFERENT DEVICE BY CHANGING TO AN OUTSIDE-IN PROCEDURE. IT WAS NOT NECESSARY TO SWITCH THE GENERAL SURGICAL TECHNIQUE OR DO A SECOND SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16051999 ↗InjuryMay 18, 2021Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT GOT AN INFECTION AFTER HE WAS TREATED WITH THE DEVICES AR-7900 (LOT: 10822462), AR-7910L (LOT: 928497924) AND AR-7523 (LOT: 934399472). THIS WAS NOTICED AFTER THE SURGERY. NO FURTHER INFORMATION RECEIVED.
Patient problems: Unspecified Infection
MAUDE report 11842500 ↗InjuryMay 18, 2021Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT GOT AN INFECTION AFTER HE WAS TREATED WITH THE DEVICES AR-7900 (LOT: 10822462), AR-7910L (LOT: 928497924) AND AR-7523 (LOT: 934399472). THIS WAS NOTICED AFTER THE SURGERY. NO FURTHER INFORMATION RECEIVED.
Patient problems: Unspecified Infection
MAUDE report 11842360 ↗
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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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