MAUDE Adverse Event Report: HOYA CORPORATION PENTAX TOKYO OFFICE PENTAX; IMAGINA HD VIDEO PROCESSOR

Model Number	EPK-I5500C
Medical Device Problem Codes	No Display/Image (1183); Optical Problem (3001)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/18/2021
Type of Reportable Event	Malfunction
Event or Problem Description
Pentax medical was made aware of an event which occurred in the pai region involving pentax video processor epk-i5500cl.In the event reported, the user states that the sales rep upgraded the firmware yesterday on 20 scopes at (b)(6) after they completed procedures.The physician called him to say that they've been having problems all morning, with various scopes, in room 3 - the room that sales personnel used to upgrade the firmware of all scopes.The issues have been image freezing, flashing, and/or going black altogether and would happen multiple times per procedure.It is occurring in each procedure so far this morning.The timing of the event is in the procedure room during use.There was no adverse event reported with this complaint.No other information provided with this complaint.
Additional Manufacturer Narrative
This device is classified as import for export, therefore 510k is not applicable.There is a similar model epk-i5500c-us is available for sale in the united states with a 510k #k190805.The device was returned to pentax for further evaluation on service order (b)(4) and is currently pending evaluation.On 14-dec-2021, a device history record (dhr) review for model epk-i5500c, (b)(4) was performed and the dhr review confirmed the endoscope was manufactured on 18feb2020 under normal conditions, passed all required inspections, and was released accordingly.The dates of approval for shipment and actual date shipped were confirmed.If additional information becomes available, a supplemental report will be filed with the new information.
Additional Manufacturer Narrative
Correction information g6: follow up #1 h2:if follow-up, what type? h3:device evaluated by manufacture.H6: coding changed based on the investigation result.Additional information: d4:unique identifier (udi).G4:premarket identification pma/510(k).Evaluation summary complaints of paused or flickering images.We are unable to determine the cause, but customer information suggests it is probably a processor issue.The cause is unknown.

• Brand Name: PENTAX
• Common Device Name: IMAGINA HD VIDEO PROCESSOR
• Manufacturer (Section D): HOYA CORPORATION PENTAX TOKYO OFFICE; tsutsujigaoka 1-1-110; akishima-shi, tokyo 196-0 012; JA 196-0012
• Manufacturer (Section G): HOYA CORPORATION PENTAX TOKYO OFFICE; tsutsujigaoka 1-1-110; akishima-shi, tokyo 196-0 012; JA 196-0012
• Manufacturer Contact: william goeller (temporary) ; 3 paragon drive; montvale, NJ 07645 ; 8004315880
• MDR Report Key: 13009020
• Report Number: 9610877-2021-01798
• Device Sequence Number: 4926108
• Product Code: PEA
• UDI-Device Identifier: 04961333233670
• UDI-Public: 04961333233670
• Combination Product (Y/N): N
• Initial Reporter State: TN
• Initial Reporter Country: US
• PMA/510(K) Number: K190805
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 12/07/2022

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
• Operator of Device: Health Professional
• Device Model Number: EPK-I5500C
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/13/2021
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/18/2021
• Supplement Date Received by Manufacturer: 11/18/2021
• Initial Report FDA Received Date: 12/15/2021
• Supplement Report FDA Received Date: 12/07/2022
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 02/18/2020
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown