DM Converter – TiN coated 01.32.3641CFRecalls & reported problems
Medacta International SA · DM Converter D/DMB - TiN coated · Class 2 · Implant
Data updated Oct 18, 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 07630971256347), received between Jun 27, 2024 and Jun 27, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 27, 2024Device Dislodged or Dislocated; Device Dislodged or Dislocated
THE PATIENT HAD A PRIMARY WITH MPACT NO HOLE CUP, MPACT DM CONVERTER AND DOUBLE MOBILITY LINER IMPLANTED ON THE (B)(6) 2024. THE CUP WAS PLACED AS USUAL, 40 INCLINATION AND ROUGHLY 20 ANTEVERSION. THE PATIENT SHOWED SIGNS OF A SPINAL DEFORMITY. THE PATIENT DISLOCATED POSTERIORLY 3 TIMES OVER IN 2 WEEKS. IT WAS FOUND THAT THE PATIENT HAD AN EXTREMELY HYPER MOBILE HIP (EXTREMELY LAX IN HER LIGAMENTS) AND HER HIP POSTERIOR CAPSULE WAS DETACHED. THE SURGEON DECIDED TO REMOVE THE MPACT NO HOLE CUP WITH DM CONVERTER LINER, THE DOUBLE MOBILITY LINER AND PUT IN A HIGHLY CONSTRAINED CUP (OF COMPETITOR). THIS WAS DONE ON THE (B)(6) 2024. THE SURGEON REPORTED THAT HE DOES NOT BELIEVE THIS WAS AN IMPLANT FAULT, THE PATIENT JUST REQUIRED A MORE CONSTRAINT HIP CONFIGURATION.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 19623329 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices
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- 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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