MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 2/10 MM L; KNEE FIXED TIBIAL INSERT

Model Number	02.12.0210CRL
Health Effect - Clinical Code	Joint Laxity (4526)
Date of Event	01/25/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Batch review performed on 01 february 2022: lot 185576: (b)(4) items manufactured and released on 18-sept-2018.Expiration date: 2023-09-04.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold with another similar reported event.
Event or Problem Description
The patient came in reporting instability and the cause of the instability is unknown.At 1 year and 7 months from the primary the surgeon revised the insert with a 13mm one and the surgery was completed successfully.
Additional Manufacturer Narrative
Batch review performed on 01 february 2022: lot 185576: (b)(4) items manufactured and released on 18-sept-2018.Expiration date: 2023-09-04.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold with another similar reported event.
Event or Problem Description
The patient came in reporting instability and the cause of the instability is unknown.At 1 year and 7 months from the primary the surgeon revised the insert with a 13mm one and the surgery was completed successfully.

• Brand Name: GMK-SPHERE TIBIAL INSERT FIXED SPHERE CR SIZE 2/10 MM L
• Common Device Name: KNEE FIXED TIBIAL INSERT
• Manufacturer (Section D): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, 6874 ; SZ 6874
• Manufacturer (Section G): MEDACTA INTERNATIONAL SA; strada regina; castel san pietro, 6874 ; SZ 6874
• Manufacturer Contact: stefano baj ; strada regina; castel san pietro, switzerland 6874 ; SZ 6874
• MDR Report Key: 13567432
• Report Number: 3005180920-2022-00129
• Device Sequence Number: 14915044
• Product Code: JWH
• UDI-Device Identifier: 07630040707190
• UDI-Public: 07630040707190
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K181635
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2022
• 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): 02/21/2022

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 Expiration Date: 09/04/2023
• Device Model Number: 02.12.0210CRL
• Device Catalogue Number: 02.12.0210CRL
• Device Lot Number: 185576
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 01/25/2022
• Initial Report FDA Received Date: 02/21/2022
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 09/18/2018
• 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