CHESAPEAKE Stabilization System 2008-90019Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10888857025455), received between Aug 5, 2022 and Aug 5, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Insert” (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 16, 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 5, 2022Difficult to Insert; Mechanical Problem; Difficult to Insert; Mechanical Problem

  IT WAS REPORTED THAT THE ANTERIOR LUMBAR DISC PREP MODULAR ANTERIOR INSERTION RAMP AND INNER SHAFT ASSEMBLY WAS TURNING ON INSERTION. THE SURGERY WAS COMPLETED SUCCESSFULLY WITH AN UNKNOWN SURGICAL DELAY. NO ADVERSE CONSEQUENCES OR MEDICAL INTERVENTION WERE REPORTED. THIS REPORT IS FOR THE INNER SHAFT ASSEMBLY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15178319 ↗