MAUDE Adverse Event Report: KARL STORZ ENDOVISION FLEXIBLE VIDEO CYSTOSCOPE

Model Number	11272VNU
Medical Device Problem Code	Contamination /Decontamination Problem (2895)
Health Effect - Clinical Code	Bacterial Infection (1735)
Date of Event	03/14/2018
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Scope was evaluated.We found there was a scrape in the working channel, but no leak.Investigation still in progress.
Event or Problem Description
Allegedly, the physician performed a cystoscopy procedure on patient.Post the procedure, patient was admitted to the icu.Patient's urine was cultured which confirmed pseudomonas aeruginosa infection.Patient was treated by an outside doctor.The clinic does not have any information on treatment, but most likely the patient received antibiotics.
Additional Manufacturer Narrative
The video scope was evaluated.We found there was a scrape in the working channel, but no associated leak.The evaluation results suggest that user error can be linked to the physical condition of the instrument.The physical evaluation of the flexible video cystoscope focused on scope damage and whether it could have an impact on patient infections.The presence of debris can harbor organisms that can lead to cross contamination between patients.Damage such as scrapes in the channel can contribute to infections; the damaged area can harbor organisms that reduce the efficacy of cleaning and subsequent reprocessing steps.In order to perform a microbiological assessment of the video cysto urethroscope (11272vnu, s/n (b)(4)), endoscope channel sampling was performed at our in-house laboratory and the resultant extract was submitted for microbial analysis on april 6, 2018.Multiple locations at the customer site were sampled in order to help determine the source of the causative organism; sterile gloves, tubes, sample containers, and water for irrigation were used.The samples were submitted to nelson laboratories to specifically determine if p.Aeruginosa was present.The final results confirm that the causative organism (p.Aeruginosa) was not present in the samples analyzed.The investigation reflects there is no direct link between the scope use/reprocessing and the patient infections as the causative organism was not recovered from any sample location.

• Brand Name: FLEXIBLE VIDEO CYSTOSCOPE
• Common Device Name: FLEXIBLE VIDEO CYSTOSCOPE
• Manufacturer (Section D): KARL STORZ ENDOVISION; 91 carpenter hill road; charlton MA 01507
• MDR Report Key: 7418170
• Report Number: 1221826-2018-00029
• Device Sequence Number: 1097825
• Product Code: FBO
• UDI-Device Identifier: 04048551226193
• UDI-Public: 4048551226193
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K062918
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Medical Assistant
• Type of Report: Initial,Followup
• Report Date (Section B): 03/19/2018

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?: No
• Operator of Device: Physician
• Device Model Number: 11272VNU
• Device Catalogue Number: 11272VNU
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/02/2018
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 03/19/2018
• Supplement Date Received by Manufacturer: 03/19/2018
• Initial Report FDA Received Date: 04/10/2018
• Supplement Report FDA Received Date: 05/22/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 69 YR