DYNACORD 222066Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20886705030009), received between Jul 8, 2024 and Dec 10, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 10, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING AN ARTHROSCOPY SURGICAL PROCEDURE, THE SURGEON WAS USING THE FREE STRAND DYNACORD BLUE W/MO-7 NDL 12PK DEVICE WITH A NEEDLE DURING AN OPEN PROCEDURE AND WHILE WHIP STITCHING A GRAFT IN PLACE THE NEEDLE CAME FLYING OFF THE SUTURE. THERE WERE NO AGGRESSIVE MOVEMENTS DURING THIS ACTION AND IT WAS NOTED THAT THE NEEDLE CAME OFF THE FREE STRAND SUTURE VERY EASILY. A COMPETITIVE SUTURE DEVICE WAS USED TO COMPLETE THE SURGERY SUCCESSFULLY. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WAS PATIENT INVOLVEMENT. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20893076 ↗
• MalfunctionJul 8, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED BY THE SALES REP IN JAPAN THAT DURING AN UNKNOWN SURGICAL PROCEDURE WITH PHILOS PERFORMED. ON (B)(6) 2024 THE DYNACORD BLUE W/MO-7 NDL 12PK DEVICE WAS APPLIED TO THE ROTATOR CUFF, THE NEEDLE PART WAS PULLED FORCEFULLY. HOWEVER, THE NEEDLE CAME OFF FROM THE SUTURE, AND THE NEEDLE LEFT IN THE BODY TEMPORARY. THE IMAGE WAS USED IMMEDIATELY, AND IT WAS ALSO VISIBLE. THE NEEDLE WAS REMOVED. THERE WAS NO DELAY IN THE PROCEDURE REPORTED. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19689302 ↗