GENESYS MATRYX 237030M5Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10845854016961), received between Jul 22, 2022 and Jul 22, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Migration or Expulsion of Device” (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.

• InjuryJul 22, 2022Migration or Expulsion of Device; Migration or Expulsion of Device

  THE SALES REPRESENTATIVE REPORTED ON BEHALF OF THE CUSTOMER THAT THE DEVICE 237030M5, GENESYS MATRYX 7.0 X 30 MM INTERFERENCE SCREW WAS BEING USED ON (B)(6) 2022 DURING A LATERAL COLLATERAL LIGAMENT & MEDIAL COLLATERAL LIGAMENT PROCEDURE WHEN IT WAS REPORTED ¿WHEN THE DOCTOR TOOK AN X-RAY AFTER THE SURGERY, OUR SCREW WAS OUT OF ITS TUNNEL.¿ FURTHER ASSESSMENT FOUND THAT ON (B)(6) 2022 AN X-RAY WAS TAKEN POST OPERATIVELY AND DISCOVERED THAT THE SCREW PULLED OUT AND DID NOT FRAGMENT. THE SECOND OPERATION WAS PERFORMED ON (B)(6) 2022, AND THE SURGEON REMOVED THE DISPLACED SCREW AND REPLACED IT WITH A ¿GENESYS SCREW 8X35 MM SCREW¿. THE PROCEDURE WAS COMPLETED WITH NO REPORT OF DELAY. THERE WAS AN EXTENDED HOSPITALIZATION OF TWO DAYS FOR THE PATIENT. IT WAS ALSO REPORTED THAT ¿THE PATIENT IS FINE". THIS REPORT IS BEING RAISED ON THE BASIS OF INJURY DUE TO THE REPORT OF SCREW PULL-OUT OF ITS TUNNEL AND A SECOND OPERATION BEING PERFORMED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15085852 ↗