TRANSCEND® 26000023Recalls & reported problems
Microport Orthopedics Inc. · COCR TRANSCEND® FEMORAL HEAD 32MM SLT TAPER LONG NECK · Class 3 · Implant
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M684260000231), received between Aug 4, 2021 and Nov 23, 2023 — classified as 3 injuries.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Device Dislodged or Dislocated1
- Insufficient Device Problem Information1
Patient problems
- Insufficient Information1
- Metal Related Pathology1
- Unspecified Infection1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryNov 23, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, PATIENT UNDERWENT L THR ON (B)(6) 2022. REVISED ON (B)(6) 2023 DUE TO INFECTION. FEMORAL HEAD AND LINER REPLACED. AUSTRALIA (B)(4).
Patient problems: Unspecified Infection
MAUDE report 18199221 ↗InjuryApr 18, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, THE GLADIATOR BIPOLAR HEAD DISLOCATED OFF OF 32MM FEMORAL HEAD.
Patient problems: Insufficient Information
MAUDE report 14134894 ↗InjuryAug 4, 2021Appropriate Device Problem Term/Code Not Available
ALLEGEDLY, PATIENT WAS REVISED DUE TO ADVERSE SOFT TISSUE REACTION TO PARTICULATE DEBRIS REVISION NJR NUMBER: (B)(4), SIDE:R, PRIMARY ASA: P2 - MILD DISEASE NOT INCAPACITATING.
Patient problems: Metal Related Pathology
MAUDE report 12275370 ↗
Other Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component) devices
- Omnifit 2001-2246Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained (metal cemented acetabular component)1 recall0 reports
- Taperloc Complete Micro Primary Femoral 51-107150Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal cemented acetabular component)41 reports
- Taperloc Complete Micro Primary Femoral 51-107140Biomet Orthopedics, LLC · Prosthesis, hip, semi-constrained (metal cemented acetabular component)36 reports
- Dynasty DSBFGD52Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)12 reports
- CONSERVE® 38AM4600Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)8 reports
- CONSERVE® 38AM4804Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)7 reports
- CONSERVE® 38AM4404Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)6 reports
- Dynasty DSBFGF56Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.