MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA CUP: MPACT 3D METAL ACETABULAR SHELL Ø56 MULTI-HOLE THIN; ACETABULAR CUP

Catalog Number	01.38.356MH
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	07/19/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Batch review performed on 02-aug-2024 lot 2212501: (b)(4) items manufactured and released on 04-aug-2022.Expiration date: 2027-07-18.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.
Event or Problem Description
The patient has a primary hip surgery on (b)(6) 2024.On (b)(6) 2024, the patient came in reporting pain and it was found that the acetabular cup had partially subsided through the acetabulum and the stem had become loose.The causes are unknown.The surgeon revised successfully all the components.Presently on (b)(6) 2024, the patient came in reporting pain due to a fractured acetabular bone.The surgeon revised the medacta cup and liner with a competitor's implants and revised the medacta head with another medacta head.The surgery was completed successfully.

• Brand Name: CUP: MPACT 3D METAL ACETABULAR SHELL Ø56 MULTI-HOLE THIN
• Common Device Name: ACETABULAR CUP
• Manufacturer (Section D): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• Manufacturer (Section G): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• Manufacturer Contact: marco giannessi ; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• MDR Report Key: 20018820
• Report Number: 3005180920-2024-00661
• Device Sequence Number: 20973937
• Product Code: LPH
• UDI-Device Identifier: 07630971212602
• UDI-Public: 07630971212602
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K202568
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Device Explanted Year: 2024
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 08/21/2024

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 Catalogue Number: 01.38.356MH
• Device Lot Number: 2212501
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/22/2024
• Initial Report FDA Received Date: 08/21/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 08/04/2022
• 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