MAUDE Adverse Event Report: DEPUY MITEK LLC US 4K C-MOUNT ENDOSCOPE, 30°, 4 MM X 167 MM, MITEK LOCK; RIGID ENDOSCOPE

Model Number 242268

Device Problems Display or Visual Feedback Problem (1184); Moisture Damage (1405)

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

Event Date 11/03/2021

Event Type  malfunction  

Manufacturer Narrative

Udi: (b)(4).To date the device has not been returned.If the device or further details are received at a later date a supplemental medwatch will be sent.

Event Description

It was reported by the sales rep that during a knee arthroscopy surgery on (b)(6) 2021, it was observed that the endoscope device had water inside of the scope that there was no visual from the device.Another like device was used to complete the procedure.There were no adverse patient consequences nor surgical delay reported.No additional information was provided.

Manufacturer Narrative

This report is being submitted in pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been able to investigate or verify prior to the required reporting date.This report does not reflect a conclusion by mitek or its employees that the report constitutes an admission that the device, mitek, 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.Investigation summary
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> the complaint device was received at the service center and evaluated.It was reported that "there is water inside of the scope and there is no visual from the device".Per service reports, this complaint can be confirmed.During the service evaluation the following defects were identified: ¿ outer tube damaged, distal tip ¿ distal tip damaged, shaver damage to distal tip ,distal tip has deposits ¿ image error, on camera, image cloudy/blurred ¿ moisture in system ¿ minor scratches on the unit the defective parts were replaced to resolve the issues.After repair, the device was found to be working according to the specifications.The faulty parts was identified as the root cause for the device failure during the service evaluation.Manufacturing record evaluation is not required as the reported event is not associated with the manufacturing process and/or the potential cause of the defect cannot be associated to manufacturing.At this point in time, no corrective action is required, and no further action is warranted.Depuy mitek will continue to track any related complaints within this device family as a means of monitoring the extent with which this complaint is observed in the field.H10: correction narrative: d3, g1: the manufacturer name and manufacturer contact facility name have been updated to reflect the correct information.

• Brand Name: 4K C-MOUNT ENDOSCOPE, 30°, 4 MM X 167 MM, MITEK LOCK
• Type of Device: RIGID ENDOSCOPE
• Manufacturer (Section D): DEPUY MITEK LLC US; 325 paramount drive; raynham MA 02767
• Manufacturer Contact: kara ditty-bovard ; 325 paramount drive; raynham, MA 02767 ; 6013142063
• MDR Report Key: 12816554
• MDR Text Key: 280872369
• Report Number: 1221934-2021-03343
• Device Sequence Number: 1
• Product Code: HRX
• UDI-Device Identifier: 10886705032075
• UDI-Public: 10886705032075
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K080560
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 11/03/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/15/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 242268
• Device Catalogue Number: 242268
• Device Lot Number: 1613636
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 03/30/2022
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 07/01/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1