MODULUS Uncemented StemRecalls & reported problems
Limacorporate SPA · Modulus modular stems (Ti6Al4V) Dia 24mm Taper B · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 08033390004862), received between Feb 18, 2026 and Feb 18, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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
- Patient Device Interaction Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 18, 2026Patient Device Interaction Problem
A SECOND REVISION TOTAL HIP ARTHROPLASTY (THA) WAS PERFORMED ON (B)(6) 2026, DUE TO LOOSENING ASSOCIATED WITH OSTEOLYSIS. DURING THE PROCEDURE, THE SURGEON EXPLANTED THE FOLLOWING DEVICES: MODULUS MOD.STEM Ø24 MM (PRODUCT CODE 431015120, LOT #1202597 AND STER. N. (B)(4), FEM. MODULAR HEAD - L Ø32MM (PRODUCT CODE 5010.09.323, LOT #1303276 AND STER. N. (B)(4), MODULUS NECK S TAPER B 12/14 (PRODUCT CODE 7590.15.030, LOT #1308590 AND STER. N. (B)(4). THE PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2013 AND THE FIRST REVISION WAS PERFORMED ON (B)(6) 2013. PATIENT IS MALE, 67 YEARS OLD WITH HIGH ACTIVITY LEVEL. EVENT HAPPENED IN JAPAN AND RELATED TO (B)(4).
Patient problems: Insufficient Information
MAUDE report 24377806 ↗
Other Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer devices
- Novation 134-36-45Exactech, Inc. · Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer2 recalls0 reports
- PINNACLE 1218-28-650Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer89 reports
- Trident 690-00-28FHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall37 reports
- Trident 690-00-22EHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall36 reports
- PINNACLE 1218-32-652Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer75 reports
- Trident 690-00-22DHowmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall22 reports
- PINNACLE 1218-32-654Depuy Orthopaedics, Inc. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer70 reports
- Trident 69-2850Howmedica Osteonics Corp. · Prosthesis, hip, constrained, cemented or uncemented, metal/polymer1 recall11 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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