MAUDE Adverse Event Report: DEPUY IRELAND - 3015516266 CENTRAL SCREW 6.0X25; SHOULDER IMPLANT - SCREW

Model Number 5500-25-600

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

Patient Problems Bone Fracture(s) (1870); Pain (1994); Discomfort (2330)

Event Date 03/01/2023

Event Type  Injury  

Manufacturer Narrative

Product complaint # (b)(4).Depuy synthes is submitting this report pursuant to the provisions of 21 cfr, part 803.This report may be based on information which depuy synthes has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by fda, depuy synthes or its employees that the report constitutes an admission that the device, depuy synthes, or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

Event Description

It was reported that the patient is being revised due to pain and discomfort in their shoulder.Dr informed that the patient felt a pop followed by pain after lifting something above their head.Dr.¿s pa informed that there may have been a fracture of the patients glenoid.Dr removed the glenoid and humeral components and opted to revise the patient with zimmer-biomet implants.Once the implants were removed, dr told the rep that he would be going with zimmer-biomet, and that he no longer needed rep's assistance in the room.There was no surgical delay.Doi: (b)(6) 2022.Dor: (b)(6) 2023.Affected side: left shoulder.

Manufacturer Narrative

Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Depuy considers the investigation closed.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.Device history lot : the product investigation found no evidence suspecting an error in the manufacturing or material that would be a contributing factor in the reported allegation(s).A manufacturing records evaluation (mre) was not performed.

• Brand Name: CENTRAL SCREW 6.0X25
• Type of Device: SHOULDER IMPLANT - SCREW
• Manufacturer (Section D): DEPUY IRELAND - 3015516266; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): DEPUY IRELAND 9616671; loughbeg, ringaskiddy co.; cork ; EI
• Manufacturer Contact: kate karberg ; 700 orthpaedic dr.; warsaw, IN 46581 ; 3035526892
• MDR Report Key: 16544467
• MDR Text Key: 311296121
• Report Number: 1818910-2023-05835
• Device Sequence Number: 1
• Product Code: PHX
• UDI-Device Identifier: 10603295548829
• UDI-Public: 10603295548829
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K212737
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 03/15/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 03/15/2023
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Model Number: 5500-25-600
• Device Catalogue Number: 550025600
• Device Lot Number: 180825
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 03/30/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 07/25/2022
• 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: 4PK LOCKING SCRW 2025 SLFDRILL; GLENOSPHERE 32+8; MODULAR UNITI BASEPLATE S 24; REVERSE HUMERAL SHELL M 36+0; REVERSE LINER 32+4 R; SHORT STEM M 36
• Patient Outcome(s): Required Intervention
• Patient Age: 64 YR
• Patient Sex: Female