MAUDE Adverse Event Report: DEPUY IRELAND - 3015516266 GLENOSPHERE 40+8; SHOULDER IMPLANT - GLENOSPHERE

Catalog Number 550540008

Device Problems Device Dislodged or Dislocated (2923); Noise, Audible (3273)

Patient Problem Joint Dislocation (2374)

Event Date 12/18/2023

Event Type  Injury  

Event Description

It was reported that the patient had the shoulder done by surgeon on (b)(6) 2023 at the hospital.Patient was picking up their grandchild and their shoulder dislocated.After reducing it with a family member, they could hear and feel a grinding in his shoulder.The surgeon felt the poly had come disassociated from the humeral shell.The grinding was the glenosphere and shell grinding together.The surgeon felt they would benefit from an exchange of the poly, humeral shell, and glenosphere.The new implants were opened and implanted and the shoulder was thoroughly washed out.Stability was confirmed and the closing process began.Unknown surgical delay.Doi: (b)(6) 2023; dor: (b)(6) 2023; affected side: right shoulder.

Manufacturer Narrative

Product complaint # (b)(4).H6 component code: appropriate term/code not available (g07002) used to capture no findings available.Investigation summary: no device associated with this report was received for examination.In order to determine if a lot related issue was possible, a worldwide complaint database search was performed.A worldwide complaint database search found no additional related reports against the provided product code/lot code combination.Based on the inability to find any additional related reports against the provided product code/lot code combination it is reasonable to conclude that there are no anomalies with regard to manufacturing or inspection contained in the device history records that would contribute to the reported event.As part of our company quality system process, all devices are manufactured, inspected, and distributed to approved specifications.Additional complaint information monitoring for potential safety signals will be conducted through complaint trending as part of the post-market surveillance.If additional information is made available, the investigation will be updated as applicable.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.This report is being submitted pursuant to the provisions of 21 cfr, part 803 (and/or part 4, as applicable).This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by depuy synthes, or its employees that the report constitutes an admission that the product, 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 report, a follow-up report will be filed as appropriate.

• Brand Name: GLENOSPHERE 40+8
• Type of Device: SHOULDER IMPLANT - GLENOSPHERE
• Manufacturer (Section D): DEPUY IRELAND - 3015516266; loughbeg ringaskiddy co.; cork ; EI
• Manufacturer (Section G): DEPUY ORTHOPAEDICS, INC. 1818910; 700 orthopaedic dr.; warsaw IN 46581 0988
• Manufacturer Contact: kate karberg ; 700 orthopaedic dr.; warsaw, IN 46581-0988 ; 3035526892
• MDR Report Key: 18433947
• MDR Text Key: 331860797
• Report Number: 1818910-2024-00068
• Device Sequence Number: 1
• Product Code: PHX
• UDI-Device Identifier: 10603295547174
• UDI-Public: 10603295547174
• 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
• Report Date: 01/02/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/03/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Catalogue Number: 550540008
• Device Lot Number: 333397
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 12/18/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 10/19/2022
• 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: REVERSE HUMERAL SHELL L 40+0; REVERSE LINER 40+0
• Patient Outcome(s): Required Intervention
• Patient Age: 70 YR
• Patient Sex: Male