MAUDE Adverse Event Report: TORNIER INC TORNIER PERFORM REVERSED LATERALIZED GLENOSPHERE +3 DIA 39MM; SHOULDER PROSTHESIS, REVERSE CONFIGURATION

Catalog Number DWJ023

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

Patient Problems Loss of Range of Motion (2032); Discomfort (2330)

Event Date 09/14/2023

Event Type  Injury  

Event Description

In the phs stemless ide study, a participant reported stiffness and discomfort in the neck and left hand.Despite receiving treatments like meloxicam and oral steroids, the symptoms persisted.Seeking a second opinion from a hand specialist, the patient underwent a steroid injection in the left ring and long fingers.Dissatisfied with the progress and care, the participant was referred to another hand surgeon for further evaluation, including pending emg and cervical mri.The patient attributes the symptoms to a previous shoulder surgery, expressing certainty that it is the root cause.

Manufacturer Narrative

Device will not be returned.If additional information becomes available, it will be provided on a supplemental report.H3 other text : device disposition unknown.

Event Description

In the phs stemless ide study, a participant reported stiffness and discomfort in the neck and left hand.Despite receiving treatments like meloxicam and oral steroids, the symptoms persisted.Seeking a second opinion from a hand specialist, the patient underwent a steroid injection in the left ring and long fingers.Dissatisfied with the progress and care, the participant was referred to another hand surgeon for further evaluation, including pending emg and cervical mri.The patient attributes the symptoms to a previous shoulder surgery, expressing certainty that it is the root cause.

Manufacturer Narrative

The reported event was not 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.A review of the device history for the reported lot did not indicate any abnormalities.No corrective actions are required at this time.No indications of material, manufacturing or design related problems were found during the investigation.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: TORNIER PERFORM REVERSED LATERALIZED GLENOSPHERE +3 DIA 39MM
• Type of Device: SHOULDER PROSTHESIS, REVERSE CONFIGURATION
• Manufacturer (Section D): TORNIER INC; 10801 nesbitt avenue s; bloomington MN 55437
• Manufacturer (Section G): TORNIER INC; 10801 nesbitt avenue s; bloomington MN 55437
• Manufacturer Contact: anna jusinski ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 18609104
• MDR Text Key: 334116952
• Report Number: 0001649390-2024-00022
• Device Sequence Number: 1
• Product Code: PHX
• UDI-Device Identifier: 00846832090389
• UDI-Public: 00846832090389
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K161742
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Study
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 03/04/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/30/2024
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Lay User/Patient
• Device Catalogue Number: DWJ023
• Device Lot Number: CZ8122042014
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 02/07/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 03/14/2022
• 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
• Patient Outcome(s): Other
• Patient Age: 73 YR
• Patient Sex: Male
• Patient Weight: 94 KG