SIGMA 9505-02-808Recalls & reported problems
Depuy (Ireland) · SIGMA HIGH PERFORMANCE PATELLA & INSERTION CASE · Class 1
- Adverse event reports
- 15
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 15 adverse event reports that list this exact device (DI 10603295229360), received between Mar 22, 2018 and Jun 17, 2022 — classified as 15 malfunctions.
The most frequently reported specific device problem is “Peeled/Delaminated” (9 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Peeled/Delaminated9
- Naturally Worn6
- Break4
- Adverse Event Without Identified Device or Use Problem3
- Crack2
- Delamination2
- Material Twisted/Bent2
Patient problems
- No Consequences Or Impact To Patient11
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 15 most recent of 15 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 17, 2022Peeled/Delaminated; Naturally Worn; Peeled/Delaminated; Naturally Worn
IT WAS REPORTED THAT INSIDE OF THE INSTRUMENT PANS WERE WORN AND FLAKING OFF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14734201 ↗MalfunctionApr 29, 2022Peeled/Delaminated; Naturally Worn; Peeled/Delaminated; Naturally Worn
IT WAS REPORTED THAT DEVICE IS LOOKING WORN AND TIRED, COATING HAS STARTED TO PEEL AWAY ON THE INSIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14256294 ↗MalfunctionMar 21, 2022Peeled/Delaminated; Peeled/Delaminated
ACCOUNT COMPLAINT THAT THE HP SIGMA PANS WERE WORN OUT. ACCOUNT WAS REQUESTING TO REPLACE THESE WORN PANS BECAUSE ACCOUNT HAD A CONCERN ON THE FLAKING OF THE INTERIORS OF THE PAN TO POSSIBLY GET INTO WOUND OF PATIENT. THEREFORE ACCOUNT REQUESTED NEW PANS. SALES CONSULTANT WAS RETURNING THESE PANS FOR A CREDIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13840508 ↗MalfunctionMar 21, 2022Peeled/Delaminated; Peeled/Delaminated
ACCOUNT COMPLAINT THAT THE HP SIGMA PANS WERE WORN OUT. ACCOUNT WAS REQUESTING TO REPLACE THESE WORN PANS BECAUSE ACCOUNT HAD A CONCERN ON THE FLAKING OF THE INTERIORS OF THE PAN TO POSSIBLY GET INTO WOUND OF PATIENT. THEREFORE ACCOUNT REQUESTED NEW PANS. SALES CONSULTANT WAS RETURNING THESE PANS FOR A CREDIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13840502 ↗MalfunctionDec 20, 2019Crack; Peeled/Delaminated; Material Twisted/Bent; Crack; Peeled/Delaminated; Material Twisted/Bent
IT WAS REPORTED THAT THE TRAYS ARE WORN AND OLD. NEED TO BE REPLACED. PLASTIC INSTRUMENT HOLDERS IN TRAYS ARE CRACKED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9506264 ↗MalfunctionDec 20, 2019Crack; Peeled/Delaminated; Material Twisted/Bent; Crack; Peeled/Delaminated; Material Twisted/Bent
IT WAS REPORTED THAT THE TRAYS ARE WORN AND OLD. NEED TO BE REPLACED. PLASTIC INSTRUMENT HOLDERS IN TRAYS ARE CRACKED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9506258 ↗MalfunctionOct 31, 2019Break; Naturally Worn; Break; Naturally Worn
IT WAS REPORTED THAT THE HP SIGMA KNEE TRAYS ARE VERY WORN. THEY HAVE COATING ON RACKS DELAMINATING WHICH COULD CAUSE STERILIZATION ISSUES. DUE TO USE AND THE TIME SPENT IN THE AUTOCLAVE, THESE INSTRUMENTS TRAYS HAVE BECOME VERY RAGGED LOOKING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9261983 ↗MalfunctionOct 31, 2019Break; Naturally Worn; Break; Naturally Worn
IT WAS REPORTED THAT THE HP SIGMA KNEE TRAYS ARE VERY WORN. THEY HAVE COATING ON RACKS DELAMINATING WHICH COULD CAUSE STERILIZATION ISSUES. DUE TO USE AND THE TIME SPENT IN THE AUTOCLAVE, THESE INSTRUMENTS TRAYS HAVE BECOME VERY RAGGED LOOKING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9261967 ↗MalfunctionOct 31, 2019Break; Naturally Worn; Break; Naturally Worn
IT WAS REPORTED THAT THE HP SIGMA KNEE TRAYS ARE VERY WORN. THEY HAVE COATING ON RACKS DELAMINATING WHICH COULD CAUSE STERILIZATION ISSUES. DUE TO USE AND THE TIME SPENT IN THE AUTOCLAVE, THESE INSTRUMENTS TRAYS HAVE BECOME VERY RAGGED LOOKING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9261965 ↗MalfunctionOct 31, 2019Break; Naturally Worn; Break; Naturally Worn
IT WAS REPORTED THAT THE HP SIGMA KNEE TRAYS ARE VERY WORN. THEY HAVE COATING ON RACKS DELAMINATING WHICH COULD CAUSE STERILIZATION ISSUES. DUE TO USE AND THE TIME SPENT IN THE AUTOCLAVE, THESE INSTRUMENTS TRAYS HAVE BECOME VERY RAGGED LOOKING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9261963 ↗MalfunctionNov 9, 2018Peeled/Delaminated; Adverse Event Without Identified Device or Use Problem; Peeled/Delaminated; Adverse Event Without Identified Device or Use Problem
THE INSTRUMENTS WERE REPORTED FOR UNKNOWN REASON.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8054925 ↗MalfunctionNov 9, 2018Peeled/Delaminated; Adverse Event Without Identified Device or Use Problem; Peeled/Delaminated; Adverse Event Without Identified Device or Use Problem
THE INSTRUMENTS WERE REPORTED FOR UNKNOWN REASON.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8054920 ↗MalfunctionNov 9, 2018Peeled/Delaminated; Adverse Event Without Identified Device or Use Problem; Peeled/Delaminated; Adverse Event Without Identified Device or Use Problem
THE INSTRUMENTS WERE REPORTED FOR UNKNOWN REASON.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8054880 ↗MalfunctionMar 22, 2018Delamination; Delamination
IT WAS REPORTED THAT THE SIGMA TRAY WAS REPLACED DUE TO PEELING. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7363624 ↗MalfunctionMar 22, 2018Delamination; Delamination
IT WAS REPORTED THAT THE SIGMA TRAY WAS REPLACED DUE TO PEELING. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7363602 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.