MAUDE Adverse Event Report: HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX; LINEAR ULTRASOUND VIDEOBRONCHOSCOPE 2.0C

Model Number EB-1970UK

Device Problem Obstruction of Flow (2423)

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

Event Date 06/27/2022

Event Type  malfunction  

Event Description

The time of event is unknown.There was no report of patient harm.Operation/suction channel clogged.

Manufacturer Narrative

We checked the returned unit and confirmed that the operation channel blocked.Based on the result, we concluded that it was caused due to the insufficient reprocessing at the facility.In addition, we confirmed that the insertion flexible tube (ift) buckled, the light guide cable buckled, the light guide cable for control body buckled, the distal body worn out, the light guide cable bump, and the insertion flexible tube (ift) dented; however, they are not the main cause, and/or irrelevant to the alleged complaint.Based on the technical report ""hr-rpt-0588(channel)"" and/or the risk analysis results, it was evaluated to submit mdr.

• Brand Name: PENTAX
• Type of Device: LINEAR ULTRASOUND VIDEOBRONCHOSCOPE 2.0C
• Manufacturer (Section D): HOYA CORPORATION PENTAX TOKYO OFFICE; tsutsujigaoka 1-1-110; akishisima-shi, tokyo 196-0 012; JA 196-0012
• Manufacturer (Section G): HOYA CORPORATION PENTAX TOKYO OFFICE; tsutsujigaoka 1-1-110; akishisima-shi, tokyo 196-0 012; JA 196-0012
• Manufacturer Contact: william goeller ; 3 paragon drive; montvale, NJ 07645
• MDR Report Key: 15071280
• MDR Text Key: 300648069
• Report Number: 9610877-2022-55292
• Device Sequence Number: 1
• Product Code: EOQ
• UDI-Device Identifier: 04961333148226
• UDI-Public: 04961333148226
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K131946
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Health Professional
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 07/21/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: EB-1970UK
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/27/2022
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 06/27/2022
• Initial Date FDA Received: 07/21/2022
• Was Device Evaluated by Manufacturer?: Yes
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1