MAUDE Adverse Event Report: ARTHREX, INC. IBAL UKA TIB BEA-RING TRL SZ 3 8MM; TEMPLATE FOR CLINICAL USE

Model Number	IBAL UKA TIB BEA-RING TRL SZ 3 8MM
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	04/19/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.The root cause of the event could not be determined from the information available and without device evaluation.If the device becomes available for evaluation, a follow-up report will be submitted.
Event or Problem Description
It was reported that the ar-601-tbc8 tibial trial broke when removing.The rep reported there were no delays caused and all fragments were retrieved.
Additional Manufacturer Narrative
Complaint confirmed.Visual inspection identified that the tibial bearing trial had fragmented, with dents around the trial body.The fragment was also received and visual inspected.Showing dents around the corner.The most likely cause is user applied mechanical forces.

• Brand Name: IBAL UKA TIB BEA-RING TRL SZ 3 8MM
• Common Device Name: TEMPLATE FOR CLINICAL USE
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• MDR Report Key: 11798861
• Report Number: 1220246-2021-03038
• Device Sequence Number: 1099282
• Product Code: HWT
• UDI-Device Identifier: 00888867037564
• UDI-Public: 00888867037564
• Combination Product (Y/N): N
• Initial Reporter State: CO
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial,Followup
• Report Date (Section B): 07/15/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: IBAL UKA TIB BEA-RING TRL SZ 3 8MM
• Device Catalogue Number: AR-601-TBC8
• Was Device Available for Evaluation?: Yes
• Initial Date Received by Manufacturer: 04/19/2021
• Supplement Date Received by Manufacturer: 04/19/2021
• Initial Report FDA Received Date: 05/10/2021
• Supplement Report FDA Received Date: 07/15/2021
• Patient Sequence Number: 1