ADVANCERecalls & reported problems across all models
Microport Orthopedics Inc. · 147 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 368
- Deaths reported
- 0
- Injuries reported
- 363
- Recalls
- 0
We found 147 models of ADVANCE by Microport Orthopedics Inc. in the FDA's device registry (GUDID). Together they are named in 368 adverse event reports in the FDA's MAUDE database, received between May 11, 2014 and Nov 24, 2025 — classified as 363 injuries, 5 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (96 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported ADVANCE problems
Device problems
- Insufficient Device Problem Information96
- Unstable96
- Loss of Osseointegration65
- Break22
- Adverse Event Without Identified Device or Use Problem18
- Appropriate Device Problem Term/Code Not Available17
- Malposition of Device17
- Detachment of Device or Device Component16
Patient problems
- No Information88
- Unspecified Infection68
- Pain59
- Insufficient Information56
- Bone Fracture(s)30
- Loss of Range of Motion24
- Failure of Implant10
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available8
ADVANCE models
147 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ADVANCE® KTCCNP30Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer20 reports
- ADVANCE® KTCCNP40Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer15 reports
- ADVANCE® KFTCNP3RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer12 reports
- ADVANCE® KPONTP35Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer12 reports
- ADVANCE® KTCCNP20Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer11 reports
- ADVANCE® KFTCNP4LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer9 reports
- ADVANCE® KIMP310RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer9 reports
- ADVANCE® KFTCNP3LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer8 reports
- ADVANCE® KIMP310LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer8 reports
- ADVANCE® KPONTP32Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer7 reports
- ADVANCE® KFTCNP4RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer6 reports
- ADVANCE® KFTCNP5RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer6 reports
- ADVANCE® KIMP410LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer6 reports
- ADVANCE® KTCCNP21Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer6 reports
- ADVANCE® KTCCNP50Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer6 reports
- ADVANCE® KFPSNP40Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer5 reports
- ADVANCE® KIMP210LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer5 reports
- ADVANCE® KIMP410RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer5 reports
- ADVANCE® KIMP412RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer5 reports
- ADVANCE® KFPSNP20Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer4 reports
- ADVANCE® KFTCNP2RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer4 reports
- ADVANCE® KFTCPC4LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer4 reports
- ADVANCE® KIMP412LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer4 reports
- ADVANCE® KIPS2410Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer4 reports
- ADVANCE® KTCCNP31Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer4 reports
- Advance KTTINP20Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer4 reports
- ADVANCE® KFPSNP30Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KFTCNN2LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KFTCNN3RProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer3 reports
- ADVANCE® KIMP210RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KIMP312RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KIMP414RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KPONTP38Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KPRC25LOProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KSP14100Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer3 reports
- ADVANCE® KSPP1512Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer3 reports
- ADVANCE® KTCCNP41Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer3 reports
- ADVANCE® K0001288ORTHOPEDIC MANUAL SURGICAL INSTRUMENT2 reports
- ADVANCE® KFCCNP2LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFDAN210Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFPAN405Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFTCNN4RProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer2 reports
- ADVANCE® KFTCNP2LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFTCNP5LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFTCNP6RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFTCPC1LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KFTCPC3LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIDH310LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIDH310RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIDH312RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP212LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP312LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP414LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP417LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP510LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP510RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP512RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP514LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP514RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIMP517RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KIPS2310Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer2 reports
- ADVANCE® KPON32MBProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KPON35MBProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer2 reports
- ADVANCE® KPON38MBProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KPONTP29Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KSP15100Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KSP18100Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® KSPP1534Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer2 reports
- ADVANCE® KTAGB410Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- Advance KTSLFM31Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer2 reports
- Advance KTSLFM40Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer2 reports
- Advance KTTINP40Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer2 reports
- ADVANCE® SPKT0024Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer2 reports
- ADVANCE® 7552001500Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® 7552002000Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® 7552002500Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® 7552003000Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® K0001015BIT, SURGICAL1 report
- ADVANCE® K0012611Guide, surgical, instrument1 report
- ADVANCE® K0031103CLAMP1 report
- ADVANCE® K0032500INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- Advance KDHR1510Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFDAN410Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFPSNP50Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFSCNP1LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFSCNP3LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFSCNP3RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFSCNP4LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFSCNP4RProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCNN3LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCNN4LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCNP1LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCPC2LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCPC3RProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCPC4RProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCPC5LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCPC5RProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer1 report
- ADVANCE® KFTCPN4RProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer1 report
- ADVANCE® KIDH110LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
- ADVANCE® KIDH210LProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer1 report
Recent ADVANCE adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjuryNov 24, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PAIN MAINLY AT NIGHT, ITCHING WHEN FALLING ASLEEP AND AT NIGHT, CONSTANT SWELLING OF THE KNEE, ALTHOUGH LESS THAN TWO YEARS AGO. SOME ALLERGIES WERE DETECTED DURING THE OPERATION: DUST, POLLEN, CHLORAMPHENICOL, PENICILLIN INTOLERANCE, AND ASPIRIN INTOLERANCE. ALLERGIES DETECTED IN TESTS PERFORMED FOR CONSTANT PAIN AND SWELLING OF THE KNEE (B)(6) 2025: POTASSIUM DICHROMATE, 2-BROMO-2-NITROPOP. 1.3, ISOPROPYLPHENOL, PARAPHENYLENEDIAMINE, LANOLIN, PROPOLIS. PATIENT SUFFERED THIS REACTION 6 YEARS. THE SURGICAL PROCEDURE IS UNCLEAR.
Patient problems: Hypersensitivity/Allergic reaction; Pain; Swelling/ Edema
MAUDE report 23633210 ↗InjuryNov 24, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PAIN MAINLY AT NIGHT, ITCHING WHEN FALLING ASLEEP AND AT NIGHT, CONSTANT SWELLING OF THE KNEE, ALTHOUGH LESS THAN TWO YEARS AGO. SOME ALLERGIES WERE DETECTED DURING THE OPERATION: DUST, POLLEN, CHLORAMPHENICOL, PENICILLIN INTOLERANCE, AND ASPIRIN INTOLERANCE. ALLERGIES DETECTED IN TESTS PERFORMED FOR CONSTANT PAIN AND SWELLING OF THE KNEE (B)(6) 2025: POTASSIUM DICHROMATE, 2-BROMO-2-NITROPOP. 1.3, ISOPROPYLPHENOL, PARAPHENYLENEDIAMINE, LANOLIN, PROPOLIS. PATIENT SUFFERED THIS REACTION 6 YEARS. THE SURGICAL PROCEDURE IS UNCLEAR.
Patient problems: Hypersensitivity/Allergic reaction; Pain; Swelling/ Edema
MAUDE report 23633209 ↗InjuryNov 24, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PAIN MAINLY AT NIGHT, ITCHING WHEN FALLING ASLEEP AND AT NIGHT, CONSTANT SWELLING OF THE KNEE, ALTHOUGH LESS THAN TWO YEARS AGO. SOME ALLERGIES WERE DETECTED DURING THE OPERATION: DUST, POLLEN, CHLORAMPHENICOL, PENICILLIN INTOLERANCE, AND ASPIRIN INTOLERANCE. ALLERGIES DETECTED IN TESTS PERFORMED FOR CONSTANT PAIN AND SWELLING OF THE KNEE (B)(6) 2025: POTASSIUM DICHROMATE, 2-BROMO-2-NITROPOP. 1.3, ISOPROPYLPHENOL, PARAPHENYLENEDIAMINE, LANOLIN, PROPOLIS. PATIENT SUFFERED THIS REACTION 6 YEARS. THE SURGICAL PROCEDURE IS UNCLEAR.
Patient problems: Hypersensitivity/Allergic reaction; Pain; Swelling/ Edema
MAUDE report 23633207 ↗InjurySep 16, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION. SRNJR NUMBER: (B)(4), SIDE: L, GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 23062513 ↗InjurySep 16, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION. SRNJR NUMBER: (B)(6) SIDE: L GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 23062510 ↗InjurySep 8, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION. SRNJR NUMBER: (B)(6). SIDE: L. GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 22999154 ↗InjurySep 8, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION. SRNJR NUMBER: (B)(6). SIDE: L. GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 22999149 ↗InjurySep 8, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO INFECTION. SRNJR NUMBER: (B)(6). SIDE: L. GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 22999148 ↗InjuryAug 20, 2025Break; Break
ALLEGEDLY, THE DISTAL PART OF THE FEMORAL COMPONENT DID BREAK OFF. ADDITIONAL, RESULTANT WEAR OCCURRED ON THE TIBIAL INSERT. THE SURGERY WAS EXTENDED MORE THAN 30 MINUTES.
Patient problems: Failure of Implant; Insufficient Information
MAUDE report 22850300 ↗InjuryJun 10, 2025Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, PATIENT WAS REVISED DUE TO ASEPTIC LOOSENING FEMUR/ASEPTIC LOOSENING TIBIA /INFECTION. SRNJR NUMBER: (B)(6), SIDE: L, GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 22178274 ↗InjuryJun 10, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT WAS REVISED DUE TO ASEPTIC LOOSENING FEMUR/ASEPTIC LOOSENING TIBIA/INFECTION. SRNJR NUMBER: (B)(6). SIDE: L. GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 22178213 ↗InjuryJun 10, 2025Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, PATIENT WAS REVISED DUE TO ASEPTIC LOOSENING FEMUR/ASEPTIC LOOSENING TIBIA/INFECTION. SRNJR NUMBER: (B)(4). SIDE: L. GENDER: F.
Patient problems: Unspecified Infection
MAUDE report 22175988 ↗InjuryJun 5, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT UNDERWENT TKA IN THE UK, DATE UNKNOWN. REVISED ON (B)(6) 2025 DUE TO INFECTION. TIBIAL INSERT REVISED WITH ANOTHER OF THE SAME SIZE. INSERT SUPPLIED UNDER SAS CATEGORY B, TGA APPROVAL REF (B)(4). NON-REVISED PRODUCTS: PORDUCT ID: KTTINP40 ADVANCE® II MODULAR TITANIUM TIBIAL BASE SZ 4 STD NONPOROUS/ LOT NO.: 1559477/ QTY: 1. PORDUCT ID: KSP16140 ADVANCE® CANAL FILLING STEM EXTENSION 17MM X 140MM/ LOT NO.: 1409427/ QTY: 1. PORDUCT ID: KFCCNP4R ADVANCE® REVISION FEMORAL SIZE 4 RIGHT NONPOROUS/ LOT NO.: 1542396/ QTY: 1. PORDUCT ID: KSP14100 ADVANCE® CANAL FILLING STEM EXTENSION 15MM X 100MM/ LOT NO.: 1409425/ QTY: 1. PORDUCT ID: KPONTP35 ADVANCE® ONLAY ALL-POLY PATELLA 35MM TRI-PEG/ LOT NO.: 1580890/ QTY: 1 AUSTRALIA (B)(4).
Patient problems: Unspecified Infection
MAUDE report 22154451 ↗InjuryApr 30, 2025Loss of Osseointegration; Loss of Osseointegration
ALLEGEDLY, EPRD REPORTED 8 NEW COMPLICATIONS FOR ADVANCE® FEMUR REVISION (1 ASEPTIC LOOSENING AND 7 DISLOCATION/INSTABILITY EVENTS). FIRST REVISION SURGERY. NO FURTHER INFORMATION WAS REPORTED. THIS INCIDENT IS CAPTURING 1 ASEPTIC LOOSENING EVENT.
Patient problems: Insufficient Information
MAUDE report 21938774 ↗InjuryMar 12, 2025Improper or Incorrect Procedure or Method; Packaging Problem; Improper or Incorrect Procedure or Method; Packaging Problem
ALLEGEDLY, WE WERE IN A RTR AND AT THE TIME OF PASSING THE FEMORAL COMPONENTS THESE GAVE US IN FEMUR 3 RIGHT STATURE AND TIBIA 3 STANDARD. THE FEMORAL COMPONENT IS RECTIFIED AND PASSED, WE CEMENTED IT AND AT THE TIME OF PLACING IT IN THE KNEE WE REALIZE THAT THIS HAD SOMETHING STRANGE AND THAT WE DID NOT HUNT, WITH THE SURGEON OBSERVED THAT THIS COMPONENT WAS NOT 3 STATURE RIGHT IF NOT LEFT, TO BUY IT WITH THE TEST COMPONENTS WE REALIZE THAT IT IS 2 STANDARD LEFT. WE RECTIFY THE BOX AND WE REALIZE THAT IN THIS INDEED IF IT WAS RIGHT THE NAME OF 3 STATURE RIGHT, BUT THE FACTORY IMPLANT WAS WRONGLY PACKAGED. THE PATIENT WAS FITTED WITH A STANDARD RIGHT 3 COMPONENT AND IT WAS A BIT TOO BIG FOR HER, WHICH MAY CAUSE LOOSENING OF THE PROSTHESIS IN THE FUTURE.
Patient problems: Insufficient Information
MAUDE report 21588223 ↗
Other Microport Orthopedics Inc. products
All Microport Orthopedics Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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