Terino Square Chin-Style I Size: MediumRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M724TSCIM1), received between Jun 23, 2022 and Jun 23, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Output Problem” (1 report).

1 other recall cover devices cleared under the same FDA submission (K902824); they may or may not involve this specific model.

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.

• InjuryJun 23, 2022Output Problem

  THIS IS THE SAME PATIENT ASSOCIATED WITH MDRS # 2028924-2022-00006 AND 2028924-2022-00009. THIS EVENT IS ASSOCIATED WITH A CHIN IMPLANT WHICH WAS EXPLANTED APPROXIMATELY 14 MONTHS POST-OP. THOUGH THE DEVICE MAY HAVE BEEN REMOVED PROPHYLACTICALLY DUE TO INFECTION CONCERNS ON THE DEVICE ASSOCIATED WITH MDR # 2028924-2022-00006, THE PATIENT/COMPLAINANT INDICATED THAT THE SURGEONS WHO REMOVED THE DEVICE HAD INDICATED THAT "EVERYTHING WAS OUT OF PLACE."

  Patient problems: Unspecified Infection

  MAUDE report 14788883 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K902824. One submission often covers many models, so check the product and lot details in each record.

• Z-2211-2013 · Aug 30, 2013 · Terminated
  Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M. To augment or reconstruct underdeveloped or traumatized mandibular region.