MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA CUP: VERSAFITCUP CC TRIO ACETABULAR SHELL CC TRIO Ø 48; HIP CEMENTLESS ACETABULAR SHELL

Catalog Number 01.26.45.0048

Device Problem Malposition of Device (2616)

Patient Problem Discomfort (2330)

Event Date 11/27/2023

Event Type  Injury  

Manufacturer Narrative

Batch review performed on 04 december 2023 lot 1910233: (b)(4) items manufactured and released on 31-march-2020.Expiration date: 2025-03-16.No anomalies found related to the problem.To date, all items of the same lot have been sold without any similar reported event during the period of review.Clinical evaluation performed by medical affairs department: revision of the cup performed at about 2 years 2 months after the primary, due to medialization of the acetabular cup and suboptimal offset.According to report, there was no loosening nor infection.From the radiographic image, the cup seems slightly medialized but the medial wall is intact.We cannot tell if this is the result of post-surgery migration or the surgeon's choice: in the latter case, no explanation for this decision was supplied.However, without a controlateral image it is difficult to evaluate the position of the cup.There is no reason to suspect a faulty device.

Event Description

At about 2 years 2 months after the primary, revision surgery performed on the left side due to medialization of the acetabular cup and suboptimal offset.Patient had discomfort since the primary surgery.No loosening of the implants.No infection.The surgeon revised successfully the cup, liner and head.

• Brand Name: CUP: VERSAFITCUP CC TRIO ACETABULAR SHELL CC TRIO Ø 48
• Type of Device: HIP CEMENTLESS ACETABULAR SHELL
• 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: 18372060
• MDR Text Key: 331094631
• Report Number: 3005180920-2023-01020
• Device Sequence Number: 1
• Product Code: LZO
• UDI-Device Identifier: 07630030807756
• UDI-Public: 07630030807756
• Combination Product (y/n): N
• Reporter Country Code: SZ
• PMA/PMN Number: K103352
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 12/21/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/21/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 01.26.45.0048
• Device Lot Number: 1910233
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 11/27/2023
• Was Device Evaluated by Manufacturer?: No
• Date Device Manufactured: 03/31/2020
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention
• Patient Age: 79 YR
• Patient Sex: Female
• Patient Weight: 66 KG