MAUDE Adverse Event Report: GLOBUS MEDICAL, INC. ANTHEM; T8 DRIVER, SR, 100MM, AO QUICK CONNECT

Model Number	6179.6008
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	Spinal Column Injury (2081)
Date of Event	02/24/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device was not available for evaluation.During a distal radius case, the tip of a t8 driver broke.It was not removed and remains in the screw head post-operatively.Due to limited inforation received and being unable to evaluate the device due to it not being returned, no determinations could be made as to the cause of the reported issue.
Event or Problem Description
It was reported that during a distal radius case, an anthem t8 driver broke at the tip which remains in the screw head post operatively. .

• Brand Name: ANTHEM
• Common Device Name: T8 DRIVER, SR, 100MM, AO QUICK CONNECT
• Manufacturer (Section D): GLOBUS MEDICAL, INC.; 2560 general armistead avenue; audubon PA 19403
• Manufacturer (Section G): GLOBUS MEDICAL, INC.; 2560 general armistead avenue; audubon PA 19403
• Manufacturer Contact: daniel paul ; 2560 general armistead avenue; audubon, PA 19403 ; 6109301800
• MDR Report Key: 18971191
• Report Number: 3004142400-2024-00059
• Device Sequence Number: 6639333
• Product Code: LXH
• UDI-Device Identifier: 00889095481594
• UDI-Public: 00889095481594
• Combination Product (Y/N): N
• Initial Reporter State: PA
• Initial Reporter Country: US
• PMA/510(K) Number: D154976
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 03/25/2024

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: 6179.6008
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/26/2024
• Initial Report FDA Received Date: 03/25/2024
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown