MAUDE Adverse Event Report: EXACTECH, INC. EQUINOXE REVERSE 38MM HUMERAL LINER +0; PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED

Catalog Number 320-38-00

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

Patient Problem Insufficient Information (4580)

Event Date 01/09/2012

Event Type  Injury  

Manufacturer Narrative

(d10) concomitant device(s): 300-01-13 - equinoxe, humeral stem primary, press fit 13mm : 1397228.320-01-38 - equinoxe reverse 38mm glenosphere : 1331329.320-10-00 - equinoxe reverse tray adapter plate tray +0 : 1410594.320-15-01 - eq rev glenoid plate : 1440647.320-15-05 - eq rev locking screw : 1242534.320-20-00 - eq reverse torque defining screw kit : 1413247.320-20-22 - eq rev compress screw lck cap kit, 4.5 x 22mm : 1427372.320-20-26 - eq rev compress screw lck cap kit, 4.5 x 26mm : 1410435.320-20-34 - eq rev compress screw lck cap kit, 4.5 x 34mm : 1402209.320-20-34 - eq rev compress screw lck cap kit, 4.5 x 34mm : 1420426.(h3) pending evaluation.

Event Description

As reported by the equinoxe shoulder study, the 75-year-old white female had a left tsa on (b)(6) 2009.The patient present with other ¿ scapular notching on (b)(6) 2012 the patient underwent standard reverse revision surgery on (b)(6) 2012.The outcome of this event is considered resolved.The case report form indicates that this event is definitely related to the device and possibly related to the procedure.This event report was received through clinical data collection activities and no device return is anticipated.

• Brand Name: EQUINOXE REVERSE 38MM HUMERAL LINER +0
• Type of Device: PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED
• Manufacturer (Section D): EXACTECH, INC.; 2320 nw 66 court; gainesville FL 32653
• Manufacturer (Section G): EXACTECH; 2320 nw 66th ct.; gainesville FL 32653
• Manufacturer Contact: matt collins ; 2320 nw 66th ct.; gainesville, FL 32653 ; 3523771140
• MDR Report Key: 19161050
• MDR Text Key: 340796006
• Report Number: 1038671-2024-00942
• Device Sequence Number: 1
• Product Code: KWT
• UDI-Device Identifier: 10885862086655
• UDI-Public: 10885862086655
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K063569
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Study,Health Professional
• Reporter Occupation: Physician
• Remedial Action: Recall
• Type of Report: Initial
• Report Date: 04/22/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 04/22/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 05/20/2013
• Device Catalogue Number: 320-38-00
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 04/03/2024
• Was Device Evaluated by Manufacturer?: No
• Date Device Manufactured: 05/21/2008
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: SEE H10
• Patient Age: 75 YR
• Patient Sex: Female
• Patient Weight: 56 KG
• Patient Race: White