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Arthrex® AR-9200SRRecalls & reported problems

Arthrex, Inc. · Sabre, 2.0mm x 7cm · Class 1

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 00888867215665), received between Nov 22, 2022 and Nov 22, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Fragmentation” (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

  • Material Fragmentation1

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.

  • MalfunctionNov 22, 2022Material Fragmentation

    ON (B)(6) 2022, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT AN AR-9200SR SABRE SHAVER WAS PLACED INTO THE JOINT AND TURNED ON, IT RELEASED METAL SHAVING PIECES. SURGEON WAS ABLE TO REMOVE ALL DEBRIS WITH A #30 SHAVER. THIS WAS DISCOVERED DURING A PROCEDURE ON (B)(6) 2022.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15842699 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.