SIGMA HIGH PERFORMANCE 9505-01-005Recalls & reported problems
Depuy (Ireland) · SIGMA HIGH PERFORMANCE FEMORAL NOTCH GUIDE SIZE 5 · Class 1
All models of SIGMA HIGH PERFORMANCE (13)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295224198), received between Jul 3, 2019 and Apr 29, 2020 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (1 report).
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
- Material Deformation1
- Material Discolored1
- Material Twisted/Bent1
- Physical Resistance/Sticking1
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 29, 2020Material Discolored; Material Twisted/Bent; Material Discolored; Material Twisted/Bent
INSTRUMENTS SHOW SIGNS OF WEAR AND DISCOLOURATIONS. NOTICED DURING CLEANING PROCESS. NO SURGICAL AFFECT. NO PATIENT AFFECT. INSTRUMENTS ARE FURTHER IN USE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10012589 ↗MalfunctionJul 3, 2019Material Deformation; Physical Resistance/Sticking; Material Deformation; Physical Resistance/Sticking
IT WAS REPORTED THAT THE SIZE 4 SIGMA NOTCH TRIAL IS STUCK IN THE SIZE 4 (LEFT) SIGMA FEMORAL COMPONENT. NO SURGICAL DELAY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8757639 ↗
Other TEMPLATE devices
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- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 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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