Arthrex® AR-7206Recalls & reported problems
Arthrex, Inc. · #2 FW W/TPR NDL 36.6MM 1/2 CIRCLE · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867041349), received between Jun 2, 2023 and Jun 2, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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 13, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 2, 2023Break; Break
ON 05/09/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA SEMS THAT AN AR-7206 FIBERWIRE NEEDLE IS BREAKING. THIS WAS DISCOVERED DURING A CASE, DEVICE BREAKS DURING USE. PER FACILITY: "USES THE WIRE WHEN CLOSING CAPSULE AFTER TOTAL HIP, AND THE NEEDLE KEEPS BREAKING. DR. FREEMAN HAS BEEN EXPERIENCING THIS ISSUE WITH MULTIPLE OF THE FIBER WIRE NEEDLES IN VARIOUS CASES. NO HARM TO PATIENT, BROKEN NEEDLES ARE DISCARDED, AND NEW ONES ARE USED TO FINISH THE CASE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17053362 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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