MAUDE Adverse Event Report: ARTHREX, INC. UNIVERSAL GLENOID - CENTRAL SCREW 15MM; SHOULDER PROSTHESIS, REVERSE CONFIGURATION

Model Number	UNIVERSAL GLENOID - CENTRAL SCREW 15MM
Health Effect - Clinical Code	No Code Available (3191)
Date of Event	05/18/2020
Type of Reportable Event	Serious Injury
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.
Event or Problem Description
It was reported that the surgeon has stated that the position of the implanted base plate is not in a proper position and therefore the surgeon decided to perform a revision surgery.During the revision surgery the surgeon decided to make an easier access to the glenoid to replace the whole prostheses.It was further reported that it was found on the x-ray that due to the position of the base plate a scapular notching was caused.The following implants were explanted: base plate ar-9500-01 (part number unknown as the provided one is incorrect).Glenosphere ar-9504s-04, stock ar-9501-08cpc, 2x periphere screws (locking) (part number unknown), central screws (locking) (part number unknown), pe-inlay (part number unknown).Update 07-jun-2020: further information were provided that the base plate was not optimally placed and the plate did not sink.During the surgery it was also discovered that the plate had good osseointegration.The size the central screw is an ar-9165-15.

• Brand Name: UNIVERSAL GLENOID - CENTRAL SCREW 15MM
• Common Device Name: SHOULDER PROSTHESIS, REVERSE CONFIGURATION
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• MDR Report Key: 10159980
• Report Number: 1220246-2020-01902
• Device Sequence Number: 3184419
• Product Code: PHX
• UDI-Device Identifier: 00888867057920
• UDI-Public: 00888867057920
• Combination Product (Y/N): N
• Initial Reporter Country: SZ
• PMA/510(K) Number: K142863
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,u
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 06/16/2020

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: Health Professional
• Device Model Number: UNIVERSAL GLENOID - CENTRAL SCREW 15MM
• Device Catalogue Number: AR-9165-15
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/25/2020
• Initial Report FDA Received Date: 06/16/2020
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other