MobiliT Cup HDM2850Recalls & reported problems
Corin Ltd · ECiMa™ insert for 28 mm head - Diam. 50 · Class 2 · Implant
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 05056139239182), received between May 20, 2025 and Mar 19, 2026 — classified as 4 injuries.
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 Problem4
Patient problems
- Unspecified Infection4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2026Adverse Event Without Identified Device or Use Problem
MOBILIT / TRINITY REVISION OF THE ECIMA INSERT AND COCR MODULAR HEAD AFTER APPROXIMATELY 3 MONTHS DUE TO INFECTION. NOTE: THIS IS A REGULARIZATION WITHIN THE FRAMEWORK OF A CLINICAL STUDY FOLLOWING A CHANGE IN OUR EVENT MONITORING PROCESS OF SAE FROM CLINICAL STUDY.
Patient problems: Unspecified Infection
MAUDE report 24636747 ↗InjuryFeb 20, 2026Adverse Event Without Identified Device or Use Problem
MOBILIT, TRINITY AND MEIJE DUO REVISION OF THE CUP, ECIMA INSERT, MODULAR HEAD AND STEM AFTER APPROXIMATIVELY 5 MONTHS AND 1 WEEK DUE TO INFECTION.NOTE 1: THIS IS THE 2ND REVISION FOR THIS PATIENT (1ST REVISION MANAGED UNDER FILE 9614209-2026-00017).NOTE 2: THE PART HLP413 IS NOT CLEARED IN THE USA.
Patient problems: Unspecified Infection
MAUDE report 24398999 ↗InjurySep 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
MOBILIT AND TRINITY REVISION OF THE ECIMA INSERT AND BIOLOX DELTA CERAMIC HEAD AFTER 1 WEEK AND 3 DAYS DUE TO INFECTION. NOTE: THIS IS A REGULARIZATION WITHIN THE FRAMEWORK OF A CLINICAL STUDY FOLLOWING A CHANGE IN OUR EVENT MONITORING PROCESS OF SAE FROM CLINICAL STUDY.
Patient problems: Unspecified Infection
MAUDE report 22962600 ↗InjuryMay 20, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
MOBILIT REVISION AND WASHOUT AFTER APPROXIMATELY 1 MONTH DUE TO INFECTION.
Patient problems: Unspecified Infection
MAUDE report 22051313 ↗
Other Prosthesis, hip, semi-constrained, uncemented, metal / polymer, non-porous, calcium 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.
How reports and recalls are matched · Editorial policy · Report an error on this page