LCS COMPLETE 2294-01-020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295110941), received between Aug 13, 2019 and Aug 13, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Loose or Intermittent Connection” (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 13, 2019Loose or Intermittent Connection; Adverse Event Without Identified Device or Use Problem; Unintended Movement; Loose or Intermittent Connection; Adverse Event Without Identified Device or Use Problem; Unintended Movement

  IT WAS REPORTED THAT THE FEMORAL TRIAL WAS LOOSE THAN USUAL AFTER CUTTING BONE WITH THE A/P RESECTION GUIDE SM+ (P/N: 900135000) DURING THE TKA SURGERY ON (B)(6) 2019. THE SURGERY WAS COMPLETED WITHOUT A SURGICAL DELAY AND THERE WAS NO ADVERSE CONSEQUENCE TO THE PATIENT. WE OBTAINED THE INVESTIGATION REQUEST WHETHER SIZE OF THE A/P RESECTION GUIDE IN QUESTION WAS DEFECTIVE ORIGINALLY OR NOT. NO FURTHER INFORMATION IS AVAILABLE.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8888014 ↗