Lineage 26010002Recalls & reported problems
Microport Orthopedics Inc. · COCR FEMORAL HEAD 22.25MM TAPER MEDIUM NECK · Class 2 · Implant
- 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 M684260100021), received between Nov 24, 2025 and Nov 24, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Insufficient Device Problem Information1
Patient problems
- Metal Related Pathology1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 24, 2025Insufficient Device Problem Information; Insufficient Device Problem Information
ALLEGEDLY, CLAIMANT (B)(6) ALLEGES THAT HE WAS IMPLANTED WITH A PHAC1212 PROFEMUR PLUS COCR MODULAR NECK (SHORT) AND A PHA00238 PROFEMUR Z FEMORAL STEM (SIZE 4) IN HIS LEFT HIP ON OR ABOUT (B)(6) 2017, IN (B)(6). IT APPEARS THAT THE IMPLANTED CUP AND LINER WERE STRYKER PRODUCTS. CLAIMANT FURTHER ALLEGES THAT HIS COBALT LEVEL MEASURED 11.6 (RESULTS DATED (B)(6) 2024) AND THAT HE WAS REFERRED TO DR. (B)(6) WHO RECOMMENDED REVISION SURGERY GIVEN CLAIMANTS SEVERELY ELEVATED METAL ION LEVELS AS WELL AS SEVERE PAIN. CLAIMANT ALLEGEDLY UNDERWENT A REVISION SURGERY ON (B)(6) 2025, AT (B)(6) HOSPITAL (REPLACEMENT COMPONENTS WERE STRYKER COMPONENTS). THE REVISION OPERATIVE NOTE STATES THAT THERE WAS TRUNNIONS AND CORROSION AT THE JUNCTION OF THE FEMORAL NECK AND COMPONENT AND THAT THE SURGEON NOTICED A FRACTURE UPON REMOVAL OF THE FEMORAL STEM, WHICH REQUIRED THE IMPLANTATION OF MULTIPLE CABLES TO FIX THE FRACTURE IN A NEAR ANATOMIC POSITION.
Patient problems: Metal Related Pathology
MAUDE report 23633133 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented devices
- NA 1365-51-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented753 reports
- NA 1365-50-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented412 reports
- ARTICUL/EZE 1365-21-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 recall280 reports
- ARTICUL/EZE 1365-11-000Depuy (Ireland) · Prosthesis, hip, semi-constrained, metal/polymer, cemented1 death262 reports
- LFIT 6260-9-236Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, metal/polymer, cemented256 reports
- PINNACLE GRIPTION 1217-32-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented2 deaths239 reports
- ELEOS™ 25002111EOnkos Surgical, Inc. · Prosthesis, hip, semi-constrained, metal/polymer, cemented3 deaths230 reports
- Novation 130-36-52Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented2 recalls124 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.