MILAGRO 231840Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886705010837), received between Jan 25, 2019 and Jan 25, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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 16, 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.

• MalfunctionJan 25, 2019Fracture; Fracture

  IT WAS REPORTED THAT DURING AN ACL REPAIR THAT THE THREADS ON THE CUSTOMER'S MILAGRO INTERFERENCE SCREW 10 X 30MM BECAME DAMAGED WHEN THE SCREW WAS BEING INSERTED INTO THE BONE TUNNEL. IT WAS REPORTED THAT DURING USE THE SURGEON DID NOT NOTCH AND THE TUNNEL WAS TOO TIGHT CAUSING TO THE SCREW TO BREAK WHEN FULLY INSERTED. THE SURGEON REMOVED THE SCREW LEAVING NOTHING IN THE PATIENT. THE SURGEON COMPLETED THE PROCEDURE WITH ANOTHER SAME TYPE SCREW IN THE SAME BONE TUNNEL WITH NO PATIENT CONSEQUENCES OR DELAYS.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8277956 ↗