ANTHEM 2187.4120Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00889095614107), received between Mar 9, 2026 and Mar 9, 2026 — classified as 1 injury.

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 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.

• InjuryMar 9, 2026Fracture

  IT WAS REPORTED THAT THIS PLATE WAS PUT INTO A PATIENT WITH A PROXIMAL TIBIA FRACTURE IN MID (B)(6) 2025. THE PATIENT ATTEMPTED TO PUT WEIGHT ON HIS RIGHT LEG TOO SOON CAUSING ANOTHER FRACTURE IN HIS RIGHT TIBIA. HE WAS BROUGHT BACK FOR ADDITIONAL SURGERY. THE INITIAL PLAN WAS TO PUT ANOTHER PLATE MEDIALLY. HOWEVER, ONCE THE SURGEON TOOK X-RAYS IN THE OPERATING ROOM, HE NOTICED THAT THE PROXIMAL TIBIA PLATE WAS BROKEN. THE PROXIMAL TIBIA PLATE WAS REMOVED DUE TO THIS. THE SURGEON STATED THAT HE DOES NOT BELIEVE THE PLATE WAS NECESSARILY THE PROBLEM, HE THINKS THE CAUSE WAS THE PATIENT PUTTING TOO MUCH PRESSURE ON THE IMPLANT TOO EARLY ON. THE SURGEON ALSO STATED THAT THIS PLATE WAS NOT SUFFICIENT FOR THE PATIENT DUE TO HIS SIZE AND THAT COULD HAVE BEEN ANOTHER CAUSE.

  Patient problems: Limb Fracture

  MAUDE report 24545144 ↗