CHESAPEAKE Stabilization System 3608-90031Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857082557), received between Aug 8, 2022 and Aug 8, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Problem” (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 8, 2022Mechanical Problem; Mechanical Problem

  IT WAS REPORTED THAT THREE (3) CHESAPEAKE CERVICAL TI 3-SCREW DRILL GUIDE INSERTERS COULD NO LONGER HOLD IMPLANTS INTRA-OPERATIVELY. THE SURGERY WAS COMPLETED SUCCESSFULLY. NO ADVERSE CONSEQUENCES, SURGICAL DELAY OR MEDICAL INTERVENTION WERE REPORTED. THIS REPORT CAPTURES THE SECOND OF THREE DRILL GUIDE INSERTERS

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15186783 ↗