TruMatch SD900.501SRecalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10886982262479), received between Jan 27, 2021 and Sep 22, 2026 — classified as 1 injury, 3 malfunctions.

The most frequently reported specific device problem is “Break” (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 16, 2026.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjurySep 22, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: Swelling/ Edema; Unspecified Infection

  MAUDE report 50856379 ↗
• MalfunctionSep 5, 2022Defective Device; Defective Device

  IT WAS REPORTED THAT DURING A PROCEDURE ON (B)(6) 2022, THE CAGE IN QUESTION WAS SHORTER THAN THE SURGEON EXPECTED. THE PROCEDURE WAS ABLE TO CONTINUE STILL USING THE IMPLANT, AND THE SURGERY WAS COMPLETED SUCCESSFULLY WITH LITTLE DELAY. THERE WAS NO ADVERSE PATIENT IMPACT. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR A TRUMATCH GRAFT CAGE-LONG BONE >5CM TO 10CM/STERILE. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15355786 ↗
• MalfunctionJan 27, 2021Break; Break

  IT WAS REPORTED THAT ON (B)(6) 2021, DURING THE IMPLANTATION OF THE CAGE, THE CAGE BROKE. THE CAGE APPEARED TO BE BRITTLE. THE SURGEON OPENED A SECOND CAGE, AND THE SECOND CAGE BROKE. THERE WAS A SURGICAL DELAY OF THIRTY (30) MINUTES. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THERE WAS NO CONSEQUENCE TO THE PATIENT. THIS REPORT INVOLVES ONE (1) TRUMATCH GRAFT CAGE-LONG BONE >5CM TO 10CM/STERILE. THIS IS REPORT 2 OF 2 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11240343 ↗
• MalfunctionJan 27, 2021Break; Break

  IT WAS REPORTED THAT ON (B)(6) 2021, DURING THE IMPLANTATION OF THE CAGE, THE CAGE BROKE. THE CAGE APPEARED TO BE BRITTLE. THE SURGEON OPENED A SECOND CAGE, AND THE SECOND CAGE BROKE. THERE WAS A SURGICAL DELAY OF THIRTY (30) MINUTES. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. THERE WAS NO CONSEQUENCE TO THE PATIENT. THIS REPORT INVOLVES ONE (1) TRUMATCH GRAFT CAGE-LONG BONE >5CM TO 10CM/STERILE. THIS IS REPORT 1 OF 2 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11240322 ↗