Skip to content

MILAGRO 231869Recalls & reported problems

Medos International Sàrl · MILAGRO ADVANCE INTERFERENCE SCREW Non-absorbable PEEK 10 x 30mm · Class 2 · Implant

All models of MILAGRO (26)

Data updated Oct 16, 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 10886705026456), received between Mar 1, 2022 and Mar 1, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Crack” (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

Device problems

  • Crack1

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.

  • MalfunctionMar 1, 2022Crack; Crack

    IT WAS REPORTED BY THE CUSTOMER IN (B)(6) THAT DURING AN ANTERIOR CRUCIATE LIGAMENT RECONSTRUCTION PROCEDURE ON (B)(6) 2022, IT WAS OBSERVED THAT THE MILAGRO ADV PEEK SCREW 10X30MM DEVICE CRACKED WHILE TRYING TO INSERT INTO TIBIAL TUNNEL. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE WITH A DELAY OF ONE MINUTE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13637547 ↗

Other FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE devices

All FASTENER, FIXATION, NONDEGRADABLE, SOFT TISSUE devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page