RECLAIM 2975-29-105Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10603295156291), received between Oct 26, 2017 and Mar 15, 2023 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Naturally Worn” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 15, 2023Device-Device Incompatibility; Naturally Worn; Device-Device Incompatibility; Naturally Worn

  IT WAS REPORTED THAT THE RECLAIM NECK TRIALS WERE NOT STAYING IN POSITION WHEN SURGEON WAS DOING FINAL TRIALING.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16550727 ↗
• MalfunctionDec 30, 2021Break; Break

  THE PROXIMAL TRIAL SHAFT BROKE DURING SURGERY. ALL PIECES WERE RECOVERED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13118669 ↗
• MalfunctionSep 18, 2018Naturally Worn; Naturally Worn

  TRIAL NECK SEGMENTS AND TRIAL BODY INSTRUMENTS ARE STRIPPED AND ARE NO LONGER SUITABLE FOR TRIAL REDUCTION PURPOSES DURING TOTAL HIP REPLACEMENT.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7886100 ↗
• MalfunctionSep 10, 2018Corroded; Corroded

  CUSTOMER REPORTS THAT THEY RECEIVED A SECOND ENTIRE HIP SET WITH RUST ON ALMOST EVERY PART OF THE KIT ON (B)(6) (THIS 2ND KIT WAS SENT TO REPLACE THE FIRST ONE SENT ON AND RECEIVED ON (B)(6) ((B)(4)). THIS KIT WENT TO CUSTOMER ON (B)(6) 2017 AND WAS NEW AT THE TIME (1ST USE), IT CAME BACK TO ST PRIEST AND WAS CHECKED ON (B)(6) 2017. THEN IT GOES TO CUSTOMER ON (B)(6) THIS YEAR. IMPACTED PRODUCTS WILL BE FILLED IN WHEN WE WILL RECEIVED THE KIT BACK ON ST PRIEST.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7859511 ↗
• MalfunctionOct 26, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  IT WAS REPORTED THAT THE RECLAIM 105MM NECK ADAPTER FROZEN WITH 22X190MM STEM REAMER.

  Patient problems: No Consequences Or Impact To Patient; No Information

  MAUDE report 6980349 ↗