MAUDE Adverse Event Report: Medacta International SA Mpact Double Mobility Shells; Mpact DM Acetabular shell Ø52

Model Number	01.32.152MB
Medical Device Problem Code	Device Dislodged or Dislocated (2923)
Health Effect - Clinical Codes	Joint Dislocation (2374); Implant Pain (4561)
Date of Event	08/25/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
At about 2 months from the primary, the patient came in presenting pain due to a dislocation of the liner from the cup and the cause is unknown.The surgeon revised the d 28/dmf liner to a same size liner and revised the 28mm biolox delta head s to a cocr ball head 12/14 d 28 mm size xl.The surgery was completed successfully.
Additional Manufacturer Narrative
Batch review performed on (b)(6) 2026 cup: mpact 01.32.152mb mpact dm acetabular shell d 52 (k143453) lot 2532982: (b)(4) items manufactured and released on 16-mar-2026.Expiration date: 02-mar-2031.No anomalies found related to the problem.To date, 71 items of the same lot have been sold with no similar reported event during the period of review.Liner: mpact dm 01.26.2852mhc double mobility hc liner d 28/dmf (k092265) lot 2530203: (b)(4) items manufactured and released on 29-jan-2026.Expiration date: 23-dec-2030.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold with no similar reported event during the period of review.Root cause: implant dislocation is possible literature described adverse event after primary joint arthroplasties and causes are often unknown.There is no indication that any potential issue with the device may have caused or contributed to the event and the investigation does not indicate any potential manufacturing related issue or systemic deficiency.

• Brand Name: Mpact Double Mobility Shells
• Common Device Name: Mpact DM Acetabular shell Ø52
• Manufacturer (Section D): Medacta International SA; strada regina; castel san pietro 6874 ; SZ 6874
• Manufacturer Contact: marco giannessi ; strada regina; castel san pietro 6874 ; SZ 6874
• MDR Report Key: 50692308
• Report Number: 3005180920-2026-00936
• Device Sequence Number: 9595238
• Product Code: LPH
• UDI-Device Identifier: 07630030860973
• UDI-Public: 07630030860973
• Combination Product (Y/N): N
• PMA/510(K) Number: K143453
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2026
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial
• Report Date (Section B): 09/09/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 01.32.152MB
• Device Lot Number: 2532982
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/25/2026
• Initial Report FDA Received Date: 09/09/2026
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 03/16/2026
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Female