RECLAIM 2975-29-095Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 10603295156284), received between Jun 20, 2018 and Jul 29, 2026 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (3 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 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 29, 2026Device-Device Incompatibility

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50074674 ↗
• MalfunctionNov 14, 2024Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT NECK AND BODY TRIALS WOULD NOT LOCK AND WOULD SPIN WHEN TRYING TO REDUCE THE HIP. THERE WAS NO DELAY IN PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20689016 ↗
• 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 16550725 ↗
• MalfunctionMay 23, 2019Break; Break

  DURING THE PROCEDURE, THE PROXIMAL PROOF TEST 95 REF: 297 529 095 BROKE THE SCREW THAT IS INSIDE THE TEST IN ORDER TO WITHDRAW THE STEM TEST! THERE WAS NO DAMAGE TO THE PATIENT AND THE SURGERY CONTINUED WITHOUT PROBLEM! PRODUCT: 297529095, LOT: NOT INFORMED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8636499 ↗
• MalfunctionMay 13, 2019Material Twisted/Bent; Material Twisted/Bent

  IT WAS REPORTED THAT DURING RECLAIM HIP REVISION, SEVERAL INSTRUMENTS HEIGHT SEGMENTS WERE DAMAGED AND NECK TRIAL SCREWS STRIPPED. A SCREW IN THE DOME OF A 40MM LINER ALSO DISLODGED. NO SURGICAL DELAY.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8605556 ↗
• MalfunctionSep 19, 2018Material Deformation; Material Deformation

  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 7890396 ↗
• MalfunctionJun 20, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PROBLEM WHILST TRIALING THE HIP WITH THE TRIAL BODY AND NECK, (2975-29-085 AND 2975-31-045) IN THAT THE 2 WERE NOT HOLDING TOGETHER IN ORDER TO SET THE VERSION ON THE TRIAL. REDUCED THE HIP TO ASSESS LENGTH, VERSION ETC, THE NECK TRIAL WAS SLIPPING AROUND THE TRIAL BODY. ON INSPECTION THE TRIAL BODY LOOKED WORN AND ¿FLATTENED¿ AT THE GROOVED SECTION WHERE THE TRIAL NECK SHOULD GRIP IT. TWO OTHER TRIAL BODIES ALSO LOOKED SIMILARLY DAMAGED. 2975-29-075, 2975-29-085, 2975-29-095. THESE ARE THE 3 WHICH APPEAR DAMAGED. THERE WAS ONLY A SLIGHT DELAY OF A FEW MINUTES DURING SURGERY, AND NO HARM CAME TO THE PATIENT.

  Patient problems: No Code Available; Not Applicable

  MAUDE report 7620453 ↗