CODMAN 20-1037Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20886704001154), received between Aug 1, 2018 and Sep 22, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 22, 2021Break; Peeled/Delaminated; Break; Peeled/Delaminated

  A FACILITY REPORTED THE SCALP CLIPS CHIPPED OFF AND BREAK DURING SURGERY. ALL THE BROKEN PARTS WERE RECOVERED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12512640 ↗
• MalfunctionAug 1, 2018Manufacturing, Packaging or Shipping Problem

  IT WAS REPORTED THAT THE RANEY SCALP CLIP CONTAINER HAD MORE THAN EXPECTED. THERE WERE 11 PRODUCTS WERE ENCLOSED IN A BOX INSTEAD OF 10 PRODUCTS WITH IN THE BOX. IT WAS CONFIRMED AT THE MEDICAL DEVICE AGENT. THERE IS NO REPORT OF PATIENT HARM. NO FURTHER INFORMATION WAS PROVIDED BY HOSPITAL. THE PRODUCT WILL BE RETURNED TO YOUR SITE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 7738560 ↗