Arthrex® AR-7572T-02Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867404557), received between Sep 23, 2026 and Sep 23, 2026 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 23, 2026Break

  On 9 Sep 2026, it was reported by an Arthrex employee via email that a AR-7572-02 STR TP 0.9mm w/2 CRVD 26.5mm NDLs WH/BLU and a AR-7572T-02 SUTURETAPE 0.9mm w/2 Curved NDLs WH/BLK 's suture broke. This was discovered upon inspection after knot tying, rendering the repair unsuccessful. This occurred during a knee ligament and meniscus repair procedure where the devices were used to repair the ligaments and the meniscus within the knee joint. There were no anomalies observed during the suturing and knot-tying process, and it appears the tape broke when tension was applied to the tissue. The surgery was completed successfully by using a product with the same part number. All of the product/fragment was removed, and nothing remains in the patient. There was no patient harm.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50867055 ↗