CORAIL L98113Recalls & reported problems
Depuy (Ireland) · CORAIL HIP SYSTEM CEMENTLESS FEMORAL STEM HA COATED REVISION 12/14 AMT 135 DEGREES HIGH OFFSET COLLAR SIZE 13 · 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 10603295262411), received between May 9, 2018 and Jan 26, 2023 — classified as 4 injuries.
The most frequently reported specific device problem is “Fracture” (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
- Adverse Event Without Identified Device or Use Problem3
- Fracture2
- Loose or Intermittent Connection1
- Osseointegration Problem1
Patient problems
- No Code Available2
- Pain2
- Bone Fracture(s)1
- Inadequate Osseointegration1
- Not Applicable1
- Physical Asymmetry1
- Scarring1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryJan 26, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ADDITIONAL INFORMATION RECEIVED. AA. WAS THERE ANY SURGICAL DELAY? WHAT WAS THE DURATION OF THE DELAY? -NO. B. WHAT IS THE AFFECTED SIDE? -RIGHT.
Patient problems: Pain; Physical Asymmetry
MAUDE report 16246515 ↗InjuryApr 24, 2019Fracture; Fracture
InjuryOct 5, 2018Fracture; Loose or Intermittent Connection; Adverse Event Without Identified Device or Use Problem; Osseointegration Problem; Fracture; Loose or Intermittent Connection; Adverse Event Without Identified Device or Use Problem; Osseointegration Problem
THE CORAIL REVISION PROSTHESIS HAS BEEN BROKEN A COUPLE OF WEEKS/MONTHS AFTER SURGERY.
Patient problems: Inadequate Osseointegration; No Code Available; Pain; Scarring
MAUDE report 7938250 ↗InjuryMay 9, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DER STATES THAT THE PATIENT FRACTURED HER FEMUR CREATING INSTABILITY IN STEM. STEM AND HEAD WERE REMOVED AND REVISED ACCORDINGLY. DOI: (B)(6) 2018; DOR: (B)(6) 2018; RIGHT HIP.
Patient problems: Bone Fracture(s); Not Applicable
MAUDE report 7497898 ↗
Other Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate devices
- Novation 130-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls156 reports
- Novation 130-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls79 reports
- CORAIL 3L92511Depuy (Ireland) · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate158 reports
- Acumatch A Series 138-36-29Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate3 recalls1 report
- Novation 136-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls43 reports
- Novation 130-32-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls33 reports
- Novation 132-32-51Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls26 reports
- Novation 136-36-53Exactech, Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate2 recalls22 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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