RECLAIM 2975-20-105Recalls & reported problems
Depuy (Ireland) · RECLAIM PROXIMAL REAMER 20mm · 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 10603295156222), received between Sep 6, 2018 and Dec 16, 2020 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Corroded” (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
Device problems
- Corroded2
- Appropriate Device Problem Term/Code Not Available1
- Break1
- Material Discolored1
- Peeled/Delaminated1
Patient problems
- No Consequences Or Impact To Patient2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 16, 2020Peeled/Delaminated; Peeled/Delaminated
RECLAIM HIP REVISION (B)(6) 2020. DURING REAMING OF THE PROXIMAL BODY THE LOOSE PARTS OF THE COULOURED RINGS WERE NOTICED. THEY USED EXTRA PULSE LAVAGE TO DECREASE THE RISK OF PARTS IN THE PATIENT.
Patient problems: Insufficient Information
MAUDE report 11024749 ↗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) (SEE (B)(4)). THIS KIT WENT TO CUSTOMER ON OCTOBER 11TH, 2017 AND WAS NEW AT THE TIME (1ST USE), IT CAME BACK TO (B)(4) AND WAS CHECKED ON OCTOBER 19TH 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 (B)(4).
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7859482 ↗MalfunctionSep 6, 2018Break; Corroded; Material Discolored; Appropriate Device Problem Term/Code Not Available; Break; Corroded; Material Discolored; Appropriate Device Problem Term/Code Not Available
AFTER RECEIVING 2 COMPLAINTS ABOUT A HIP KIT ORTHOKIT MANAGER CHECKED THE BUILD 5 IN THE WAREHOUSE, AND SAW RUST ON ALMOST EVERY PART OF THE KIT. FOR SOME PARTS IT'S ALSO MISSING COLOR CODES (USUALLY RED, YELLOW, GREEN, BLUE). THIS KIT WENT TO A CUSTOMER IN (B)(6) 2016 AND WAS NEW AT THE TIME. IT WAS CHECKED WHEN IT CAME BACK IN 2016 AND WAS LET IN STORAGE SINCE THEN.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7850183 ↗
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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