Locking Cap, 2.7mm MDS100301LRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10812269021767), received between Jan 31, 2018 and Jan 31, 2018 — classified as 2 injuries.

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

• InjuryJan 31, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE OPERATING SURGEON REPORTED THAT REMOVAL OF THE SUBJECT DEVICE AND ACCOMPANYING IMPLANTS HAD BEEN SCHEDULED DUE TO CREPITUS OF THE FPL TENDON. THE ORIGINAL SURGERY TOOK PLACE ON (B)(6) 2017. THE REMOVAL PROCEDURE WAS COMPLETED ON (B)(6) 2018 WITH NO COMPLICATIONS REPORTED. ALL IMPLANTS WERE INTACT AND RETURNED TO THE MANUFACTURER FOR EVALUATION.

  Patient problems: Missing Value Reason

  MAUDE report 7230769 ↗
• InjuryJan 31, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE OPERATING SURGEON REPORTED THAT REMOVAL OF THE SUBJECT DEVICE AND ACCOMPANYING IMPLANTS HAD BEEN SCHEDULED DUE TO CREPITUS OF THE FPL TENDON. THE ORIGINAL SURGERY TOOK PLACE ON (B)(6) 2017. THE REMOVAL PROCEDURE WAS COMPLETED ON (B)(6) 2018 WITH NO COMPLICATIONS REPORTED. ALL IMPLANTS WERE INTACT AND RETURNED TO THE MANUFACTURER FOR EVALUATION.

  Patient problems: Missing Value Reason

  MAUDE report 7230707 ↗