PHYSICA KR Right Tibial LinerRecalls & reported problems
Limacorporate SPA · KR Liner Right #7 - h. 14 · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390088954), received between Mar 16, 2026 and Mar 16, 2026 — classified as 1 injury.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 16, 2026Adverse Event Without Identified Device or Use Problem
REVISION SURGERY WAS PERFORMED ON (B)(6) 2022 TO RESTORE KNEE FUNCTIONALITY AFTER REMOVAL OF TIBIAL LINER. ORIGINAL SURGERY OCCURRED ON (B)(6) 2018 TO IMPLANT PHYSICA KR KNEE SYSTEM CONSISTING OF FOLLOWING COMPONENTS: - PHYSICA KR FEMUR COMP.RIGHT #8 (PART NUMBER 6511.09.180, LOT 16AS039, STERILIZATION (B)(4)), - PHYSICA FIXED TIBIAL PLATE #7 (PART NUMBER 6522.15.070, LOT 1801260, STERILIZATION (B)(4)), - PHYSICA KR TIB. LINER RIGHT #7 (PART NUMBER 6531.50.714, LOT 14L0090, STERILIZATION (B)(4)). PATIENT STARTED TO HAVE BURSITIS, AND AT A FOLLOW-UP APPOINTMENT STATED SHE WAS FALLING BECAUSE OF HER KNEE AND CONTINUED PAIN. INITIALLY SHE TRIED PHYSICAL THERAPY AND A KNEE BRACE BUT CONTINUED TO HAVE FALLS AND PAIN. X-RAY SCAN DID NOT SHOW LOOSENING ACCORDING TO MEDICAL TEAM. ABOVE MENTIONED LINER WAS EXPLANTED ON (B)(6) 2021. PATIENT IS FEMALE. THE EVENT OCCURRED IN THE UNITED STATES.
Patient problems: Implant Pain
MAUDE report 24603382 ↗
Other Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer devices
- R3 71363077Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER461 reports
- NA 71364009Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER174 reports
- JOURNEY 74012415Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER163 reports
- JOURNEY 74012416Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER163 reports
- JOURNEY 74012414Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER129 reports
- GENESIS II 71440194Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER114 reports
- GENESIS II 71440842Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER113 reports
- JOURNEY 74018901Smith & Nephew, Inc. · PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER106 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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