TRANSCEND® 26000022Recalls & reported problems
Microport Orthopedics Inc. · COCR TRANSCEND® FEMORAL HEAD 32MM SLT TAPER MEDIUM NECK · Class 3 · Implant
All models of TRANSCEND (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI M684260000221), received between Mar 11, 2020 and Jul 15, 2021 — classified as 5 injuries.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component2
- Appropriate Device Problem Term/Code Not Available1
- Device Dislodged or Dislocated1
- Material Fragmentation1
Patient problems
- Metal Related Pathology2
- No Information2
- Unspecified Tissue Injury1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJul 15, 2021Appropriate Device Problem Term/Code Not Available
ALLEGEDLY, PATIENT REVISED DUE TO EVIDENCE OF PSEUDOTUMOR AND CORROSION. CHANGES ON THE FEMALE SIDE OF THE TAPER AND ON THE MALE SIDE TO A LESSER DEGREE (RIGHT HIP).
Patient problems: Metal Related Pathology
MAUDE report 12178721 ↗InjuryJul 15, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated
ALLEGEDLY, PATIENT REVISED DUE TO COPIOUS AMOUNT OF BLACK DISCOLORED TISSUE, BLACK DISCOLORATION OF THE JOINT CAPSULE CONSISTENT WITH METALLOSIS AND DISLOCATION. (LEFT HIP)
Patient problems: Unspecified Tissue Injury
MAUDE report 12178695 ↗InjuryFeb 9, 2021Material Fragmentation
ALLEGEDLY, THE PATIENT HAD METAL ON METAL COMPLICATIONS.
Patient problems: Metal Related Pathology
MAUDE report 11300680 ↗InjuryMar 11, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, THE PATIENT FELL AND DISLOCATED, DURING CLOSED REDUCTION THE BIPOLAR DISASSOCIATED, AND THEN THE PATIENT WAS REVISED. REFERENCE (B)(4).
Patient problems: No Information
MAUDE report 9821732 ↗InjuryMar 11, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, PATIENT FELL AGAIN, DISLOCATED AND THE BIPOLAR DISASSOCIATED. THERE HAS NOT BEEN A CONFIRMED REVISION FOR THIS INCIDENT. REFERENCE (B)(4) AS A PREVIOUS INCIDENT FOR THIS PATIENT.
Patient problems: No Information
MAUDE report 9817320 ↗
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
- CONSERVE® 38AM4635Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)5 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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