ALIF VERTIGRAFT 273513520Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034190884), received between Aug 16, 2021 and Aug 16, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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.

• MalfunctionAug 16, 2021Device-Device Incompatibility; Device-Device Incompatibility

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT DURING A PROCEDURE ON (B)(6) 2021, THE INSERTER WOULD USUALLY CATCH THEN YOU TURN THE END TO TIGHTEN THE IMPLANT ON HOWEVER THIS WOULD NOT WORK. THE ISSUE WAS RESOLVED WITH HOSPITAL SET. THERE WAS NO DELAY TO SURGERY OR PATIENT IMPACT. NO FURTHER INFORMATION PROVIDED. THIS REPORT IS FOR ONE (1) UNIVERSAL ALIF INSTRUMENT SET VERTIGRAFT INSERTER SHAFT THIS IS REPORT 2 OF 3 FOR COMPLAINT (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12328274 ↗