MAUDE Adverse Event Report: TORNIER S.A.S. AEQUALIS PERFORM GLENOID; PROSTHESIS SHOULDER JOINT POLYMER

Model Number UNKNWON

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Tissue Breakdown (2681)

Event Date 05/04/2021

Event Type  Injury  

Manufacturer Narrative

Once the investigation has been completed any additional information will be reported in a supplemental report.

Event Description

Revision booked on 18 may for an aequalis ascend flex humeral head and an aequalis perform glenoid anatomic arthoplasty.Will remove the humeral head and glenoid components and replace them with a perform reverse glenoid and humeral tray and poly as the patient has experienced a cuff tear.

Event Description

Revision booked on 18 may for an aequalis ascend flex humeral head and an aequalis perform glenoid anatomic arthoplasty.Will remove the humeral head and glenoid components and replace them with a perform reverse glenoid and humeral tray and poly as the patient has experienced a cuff tear.

Manufacturer Narrative

The reported event could not be confirmed, since the device was not returned for evaluation and no other evidences were provided.The device inspection was not possible as the product was not returned for investigation.The device history record could not be reviewed because the affected device was not returned, and the lot number was not communicated.A review of the labeling did not indicate any abnormalities.More detailed information about the complaint event as well as the affected device must be available in order to determine the root cause of the complaint event.If device is returned or any further information is provided, the investigation report will be reassessed.

• Brand Name: AEQUALIS PERFORM GLENOID
• Type of Device: PROSTHESIS SHOULDER JOINT POLYMER
• Manufacturer (Section D): TORNIER S.A.S.; 161 rue lavoisier; montbonnot saint-martin 38330 ; FR 38330
• MDR Report Key: 11960600
• MDR Text Key: 255194068
• Report Number: 3000931034-2021-00272
• Device Sequence Number: 1
• Product Code: KWS
• Combination Product (y/n): N
• PMA/PMN Number: K111902
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Type of Report: Initial,Followup
• Report Date: 10/12/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/08/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Lay User/Patient
• Device Model Number: UNKNWON
• Device Catalogue Number: UNK_WTM
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 09/13/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention