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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

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Sources and updates

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