MAUDE Adverse Event Report: DEPUY IRELAND - 3015516266 CS META SCREW DEPTH GAUGE; SHOULDER INSTRUMENT - DEPTH GAUGE

Model Number 2317-70-017

Device Problems Mechanical Jam (2983); No Apparent Adverse Event (3189)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 01/09/2023

Event Type  malfunction  

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 sliding depth gauge would not slide.

Manufacturer Narrative

Product complaint # (b)(4).Mfr# 1818910-2023-01525 is being retracted since it was found to be a duplicate of mfr#1818910-2023-01443.Mfr# 1818910-2023-01443 will be kept for investigation purposes.

• Brand Name: CS META SCREW DEPTH GAUGE
• Type of Device: SHOULDER INSTRUMENT - DEPTH GAUGE
• 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: 16206769
• MDR Text Key: 308126512
• Report Number: 1818910-2023-01525
• Device Sequence Number: 1
• Product Code: HTJ
• UDI-Device Identifier: 10603295532613
• UDI-Public: 10603295532613
• Combination Product (y/n): N
• Reporter Country Code: US
• 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: 01/19/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/19/2023
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 2317-70-017
• Device Catalogue Number: 231770017
• Device Lot Number: PR160558
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 01/20/2023
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 07/06/2021
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1