MAUDE Adverse Event Report: SYNTHES GMBH 2.8MM THRDD GUIDE F/ 3.5MM SCR VA AND LCP; GUIDE, SURGICAL, INSTRUMENT

Catalog Number 03.133.004

Device Problems Device-Device Incompatibility (2919); Material Twisted/Bent (2981)

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

Event Date 01/22/2024

Event Type  malfunction  

Manufacturer Narrative

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 the information is unknown, not available or does not apply, the section/field of the form is left blank.D9: complainant part is expected to be returned for manufacturer review/investigation, but has yet to be received.E3: initial reporter is a synthes employee.H3, h4, h6: without a lot number the device history records review could not be completed.Product was not returned.Based on the information available, it has been determined that no corrective and/or preventative action is proposed.This complaint will be accounted for and monitored via post market surveillance activities.If additional information is made available, the investigation will be updated as applicable.Device was used for treatment, not diagnosis.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 on (b)(6) 2024 during an unknown procedure, the threaded drill guides in question would not thread into the proximal humerus locking plate.The surgeon tried with multiple threaded drill guides and all had trouble threading into the plate.The procedure was completed successfully without any surgical delay.No adverse patient impact was reported.No further information is available to report.This report is for a 2.8mm thrdd guide f/ 3.5mm scr va and lcp.This is report 4 of 10 for (b)(4).

Manufacturer Narrative

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.D10: therapy date for all concomitant products is (b)(6) 2024.Device was used for treatment, not diagnosis.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.

• Brand Name: 2.8MM THRDD GUIDE F/ 3.5MM SCR VA AND LCP
• Type of Device: GUIDE, SURGICAL, INSTRUMENT
• Manufacturer (Section D): SYNTHES GMBH; eimattstrasse 3; oberdorf 4436 ; SZ 4436
• Manufacturer (Section G): MONUMENT; 1101 synthes avenue; monument CO 80132
• Manufacturer Contact: kate karberg ; 1302 wright lane east; west chester, PA 19380 ; 3035526892
• MDR Report Key: 18640017
• MDR Text Key: 334537951
• Report Number: 8030965-2024-01914
• Device Sequence Number: 1
• Product Code: FZX
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: EXEMPT
• 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

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 02/05/2024
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 03.133.004
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 03/12/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• 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
• Treatment: 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP; 2.8 THRDD GUIDE F/ 3.5 SCR VA AND LCP