RECLAIM 2976-17-140Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295156543), received between Sep 5, 2018 and Aug 23, 2022 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Failure to Cut” (2 reports).

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 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionAug 23, 2022Break; Break

  IT WAS REPORTED THAT THE RECLAIM 17 X 140 REAMER BROKE AT ATTACHMENT POINT, 2 SMALL BREAKS ON THE REAMER WHERE THE HANDLE ATTACHES TO THE REAMER. THERE WAS NO SURGICAL DELAY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15277728 ↗
• MalfunctionAug 4, 2022Failure to Cut; Failure to Cut

  DISTAL REAMERS ARE DULL AND NEED REPLACED. THE PROCEDURE WAS COMPLETED WITHOUT COMPLICATIONS. NO PATIENT CONSEQUENCES OR ADVERSE EVENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15162861 ↗
• MalfunctionAug 4, 2022Failure to Cut; Failure to Cut

  DISTAL REAMERS ARE DULL AND NEED REPLACED. THE PROCEDURE WAS COMPLETED WITHOUT COMPLICATIONS. NO PATIENT CONSEQUENCES OR ADVERSE EVENTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15162782 ↗
• MalfunctionSep 5, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CUSTOMER REPORTS TO HIS SALES REPRESENTATIVE ON (B)(6) THAT THEY RECEIVED AN ENTIRE HIP SET WITH RUST ON ALMOST EVERY PART OF THE KIT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7847026 ↗