CHESAPEAKE® Stabilization System 2013-21136L15Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857027473), received between Mar 15, 2021 and Mar 15, 2021 — 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.

• MalfunctionMar 15, 2021Mechanical Problem; Mechanical Problem

  A PHYSICIAN REPORTED THAT A CHESAPEAKE SCREW PLACED IN THE MIDLINE POSITION WAS THREADED ALL THE WAY THROUGH THE CHESAPEAKE CAGE INTO THE VERTEBRAL BODY. THE PHYSICIAN REMOVED THE LATERAL SCREWS AND THE CAGE BEFORE REMOVING THE MIDLINE SCREW. A SECOND CAGE AND TWO NEW LATERAL SCREWS WERE IMPLANTED AND, "THE SAME ISSUE OCCURRED FOR A SECOND TIME." THE SECOND CAGE AND LATERAL SCREWS REMAIN IMPLANTED IN THE PATIENT AND, "THE MIDLINE SCREW STILL WITHIN THE CAGE, BUT NOT TORQUED OFF." THERE WAS A 45-MINUTE SURGICAL DELAY. THIS REPORT CAPTURES THE 2ND CAGE WHICH REMAINS IMPLANTED IN THE PATIENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11489917 ↗