CORAIL L98010Recalls & reported problems
Depuy (Ireland) · CORAIL HIP SYSTEM CEMENTLESS FEMORAL STEM HA COATED REVISION 12/14 AMT 135 DEGREES STANDARD COLLAR SIZE 10 · Class 2 · Implant
All models of CORAIL (121)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10603295262299), received between May 6, 2021 and Mar 13, 2024 — classified as 4 injuries.
The most frequently reported specific device problem is “Fracture” (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. 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
- Fracture1
- Loss of or Failure to Bond1
- Migration1
- Osseointegration Problem1
Patient problems
- Ambulation or Postural Difficulties1
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bone Fracture(s)1
- Fall1
- Inadequate Osseointegration1
- Limb Fracture1
- Pain1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMar 13, 2024Osseointegration Problem; Migration; Osseointegration Problem; Migration
IT WAS REPORTED THAT THE PATIENT RECEIVED A THA (B)(6) 2024 AFTER A NAIL REMOVAL THAT CUT THROUGH THE FEMORAL HEAD. PATIENT FELL ON 2/16 AND DISLOCATED HER HIP. THEY WERE NOT ABLE TO REDUCE IN THE ED SO BROUGHT BACK TO OPERATING ROOM. APPEARED STEM SUBSIDED FROM FALL AND WAS LOOSE. STEM AND DUAL MOBILITY WAS REVISED TO CEMENTED ENDURANCE STEM AND CONSTRAINED LINER. DOI: (B)(6) 2024. DOR: (B)(6) 2024. AFFECTED SIDE : RIGHT HIP.
Patient problems: Fall; Inadequate Osseointegration
MAUDE report 18893539 ↗InjuryMar 22, 2023Fracture; Fracture
BROKEN POST-OP. PATIENT UNDERWENT A RIGHT TOTAL HIP REVISION PROCEDURE ON (B)(6) 2022 WHERE A CORAIL REV STEM WAS IMPLANTED. ABOUT 7 MONTHS AFTER IMPLANTATION, THE STEM WAS BROKEN. THE PATIENT IS CURRENTLY SEEKING THE CONTINUED TREATMENT AT ANOTHER HOSPITAL.
Patient problems: Ambulation or Postural Difficulties; Limb Fracture; Pain
MAUDE report 16590552 ↗InjuryApr 4, 2022Loss of or Failure to Bond; Loss of or Failure to Bond
REVISION COMPLETED DUE TO LOOSENING SECONDARY TO HIP FRACTURE.
Patient problems: Bone Fracture(s)
MAUDE report 13995922 ↗InjuryMay 6, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
PATIENT WAS REVISED TO TREAT INFECTION. ALL COMPONENTS REMOVED. DOI: (B)(6) 2021 DOR: (B)(6) 2021, UNK HIP.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11783185 ↗
Other Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented devices
- BIOLOX DELTA 1365-32-310Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented551 reports
- PINNACLE ALTRX 1221-36-052Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented481 reports
- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
- BIOLOX DELTA 1365-36-720Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death189 reports
- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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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