MAUDE Adverse Event Report: OLYMPUS WINTER & IBE GMBH OUTER SHEATH, 26 FR., 2 STOPCOCKS, ROTATABLE; RESECTION SHEATHS, CYSTOSCOPE SHEATHS, HYSTEROSCOPE SHEATHS

Model Number	A22026A
Medical Device Problem Code	Obstruction of Flow (2423)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/06/2023
Type of Reportable Event	Serious Injury
Event or Problem Description
Olympus was informed that during therapeutic transurethral resection of the prostate (turp) procedure, the user experienced poor outflow, which resulted in poor vision and the equipment was exchanged to a competitors equipment.This led to a prolongation of approximately 30-40 minutes.However, the procedure was successfully completed with the competitors equipment.An olympus representative was onsite during 5-6 similar procedures to help fix the problem but could not succeed.
Additional Manufacturer Narrative
The suspect medical device has not yet been returned to olympus for evaluation/investigation.Therefore, the exact cause of the patient's outcome and the reported phenomenon could not be determined and is being judged as unknown.However, if the suspect medical device is returned for evaluation/investigation or additional significant information becomes available, this report will be updated.
Additional Manufacturer Narrative
This supplemental report was submitted to provide the results of the investigation from the legal manufacturer.The reported dissatisfaction with the vision in the surgical field is most likely not attributable to the user of the outer resectoscope sheath.Defects or the like of the outer sheath were not specified.Instead, it is likely that the dissatisfaction with the visibility is directly related to the irrigation system chosen by the customer.It was further reported the customer did not use a pump was not used for fluid management as normal saline was free flow.The lot number for the subject device could not be obtained and was not provided by the customer; therefore, a device history records could not be reviewed.Olympus will continue to monitor complaints for this device.

• Brand Name: OUTER SHEATH, 26 FR., 2 STOPCOCKS, ROTATABLE
• Common Device Name: RESECTION SHEATHS, CYSTOSCOPE SHEATHS, HYSTEROSCOPE SHEATHS
• Manufacturer (Section D): OLYMPUS WINTER & IBE GMBH; kuehnstrasse 61; hamburg, hamburg 22045 ; GM 22045
• Manufacturer (Section G): OLYMPUS WINTER & IBE GMBH; kuehnstrasse 61; hamburg
• Manufacturer Contact: daniel wladow ; kuehnstrasse 61; hamburg 22045 ; GM 22045 ; 4940669662955
• MDR Report Key: 16494998
• Report Number: 9610773-2023-00671
• Device Sequence Number: 6366391
• Product Code: GCP
• UDI-Device Identifier: 04042761029346
• UDI-Public: 04042761029346
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K790071
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility,Company Representative,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 04/27/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: A22026A
• Device Catalogue Number: A22026A
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 02/06/2023
• Supplement Date Received by Manufacturer: 03/30/2023
• Initial Report FDA Received Date: 03/07/2023
• Supplement Report FDA Received Date: 04/27/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: UNSPECIFIED OLYMPUS TELESCOPE
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown