MAUDE Adverse Event Report: MEDACTA INTERNATIONAL SA GMK-SPHERE 02.12.0610FL TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/10 MM L

Model Number	02.12.0610FL
Health Effect - Clinical Code	Pain (1994)
Date of Event	01/25/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Batch review performed on 01 february 2022: lot 1902487: (b)(4) items manufactured and released on 03-june-2019.Expiration date: 2024-05-15.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold without any similar reported event.
Event or Problem Description
The patient came in reporting anterior knee pain and the cause is unknown.The surgeon resurfaced the patient's natural patella and revised the poly.The surgery was completed successfully.Implanted components: 02.12.E0610fl gmk-sphere tibial insert e-cross - flex 6l -10mm 2012410.02.07.0034rp patella resurfacing s2 2111891.
Additional Manufacturer Narrative
Batch review performed on 01 february 2022: lot 1902487: (b)(4) items manufactured and released on 03-june-2019.Expiration date: 2024-05-15.No anomalies found related to the problem.To date, (b)(4) items of the same lot have been sold without any similar reported event.
Event or Problem Description
The patient came in reporting anterior knee pain and the cause is unknown.The surgeon resurfaced the patient's natural patella and revised the poly.The surgery was completed successfully.Implanted components: 02.12.E0610fl gmk-sphere tibial insert e-cross - flex 6l -10mm 2012410.02.07.0034rp patella resurfacing s2 2111891.

• Brand Name: GMK-SPHERE 02.12.0610FL TIBIAL INSERT FIXED SPHERE FLEX SIZE 6/10 MM L
• Common Device Name: TIBIAL INSERT FIXED
• 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: 13567342
• Report Number: 3005180920-2022-00130
• Device Sequence Number: 20295692
• Product Code: JWH
• UDI-Device Identifier: 07630030826931
• UDI-Public: 07630030826931
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K121416
• 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: 05/15/2024
• Device Model Number: 02.12.0610FL
• Device Catalogue Number: 02.12.0610FL
• Device Lot Number: 1902487
• 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: 06/03/2019
• 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: Male