RECLAIM 34-185-0020Recalls & reported problems
Depuy (Ireland) · RECLAIM MONOBLOC – REVISION HIP SYSTEM MONOBLOC DISTAL REAMER STANDARD 20 · Class 1
All models of RECLAIM (149)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10603295536154), received between Dec 14, 2023 and Dec 20, 2023 — classified as 3 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.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility3
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 20, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE RECLAIM MONOBLOC REAMER WAS STUCK IN THE CANAL. WE TRIED TO REMOVE THE REAMER BY USING THE DRILL AND WERE UNSUCCESSFUL. THEY THEN TRIED USING THE T-HANDLE AND THEN THE CURVED EXTRACTOR. ALL THREE OPTIONS WERE UNSUCCESSFUL. THEY WERE FINALLY ABLE TO EXTRACT THE REAMER AFTER 10 MIN. THE REAMER THAT GOT STUCK WAS THE SIZE 19 STANDARD.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18365708 ↗MalfunctionDec 14, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE RECLAIM MONOBLOC REAMERS WHEN TRIALING SPIN SO WE WERE UNABLE TO RELOCATE THE TRIALS TO THE CUP.
Patient problems: Insufficient Information
MAUDE report 18325991 ↗MalfunctionDec 14, 2023Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE RECLAIM MONOBLOC REAMERS WHEN TRIALING SPIN SO WE WERE UNABLE TO RELOCATE THE TRIALS TO THE CUP.
Patient problems: Insufficient Information
MAUDE report 18325941 ↗
Other REAMER devices
- QUICKSET 2440-00-551Depuy (Ireland) · REAMER1,150 reports
- QUICKSET 2440-00-549Depuy (Ireland) · REAMER1,113 reports
- QUICKSET 2440-00-553Depuy (Ireland) · REAMER1,105 reports
- QUICKSET 2440-00-547Depuy (Ireland) · REAMER1,073 reports
- QUICKSET 2440-00-555Depuy (Ireland) · REAMER1,065 reports
- QUICKSET 2440-00-557Depuy (Ireland) · REAMER1,031 reports
- QUICKSET 2440-00-545Depuy (Ireland) · REAMER947 reports
- QUICKSET 2440-00-552Depuy (Ireland) · REAMER888 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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