MAUDE Adverse Event Report: TORNIER S.A.S. AEQUALIS REVERSED GLENOID BASEPLATE; SHOULDER JOINT METAL PROSTHESIS

Model Number	DIAM. 25MM THREADED POST
Medical Device Problem Codes	Break (1069); Loosening of Implant Not Related to Bone-Ingrowth (4002)
Health Effect - Clinical Codes	Bone Fracture(s) (1870); Failure of Implant (1924); Inadequate Osseointegration (2646)
Date of Event	10/16/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
This is the initial report submitted regarding this surgical event and medical device.The information contained in this report is being provided to the fda to comply with regulations regarding medical device reporting and is based on information submitted by others that may or may not be factually correct.
Event or Problem Description
Visit date on (b)(6) 2018 (onset date of adverse event: (b)(6) 2017).Post-operative complication: humeral fracture / injury (traumatic).Trauma on left shoulder : 1 screw broken and loosening of glenoïd.No surgical procedure at that time.(b)(6) 2018: revision surgery for implant breakage on the glenoid side.
Additional Manufacturer Narrative
This is the final report submitted regarding this surgical event and medical device.The information contained in this report is being provided to the fda to comply with regulations regarding medical device reporting and is based on information submitted by others that may or may not be factually correct.This submission does not constitute a determination or admission that a device has malfunction or is related to a death or injury.
Event or Problem Description
Trauma on left shoulder: 1 screw broken and loosening of glenoid.(b)(6) 2018: revision surgery.Subject: (b)(6).

• Brand Name: AEQUALIS REVERSED GLENOID BASEPLATE
• Common Device Name: SHOULDER JOINT METAL PROSTHESIS
• Manufacturer (Section D): TORNIER S.A.S.; 161 rue lavoisier; montbonnot saint martin, 38330 ; FR 38330
• MDR Report Key: 10464814
• Report Number: 3000931034-2020-00102
• Device Sequence Number: 19612836
• Product Code: KWS
• UDI-Device Identifier: 03700386952661
• UDI-Public: 03700386952661
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K132285
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2018
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: study
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/30/2020

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: Lay User/Patient
• Device Expiration Date: 12/11/2020
• Device Model Number: DIAM. 25MM THREADED POST
• Device Catalogue Number: DWE730
• Device Lot Number: AA1438
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 07/30/2020
• Supplement Date Received by Manufacturer: 07/30/2020
• Initial Report FDA Received Date: 08/28/2020
• Supplement Report FDA Received Date: 10/02/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 71 YR