MAUDE Adverse Event Report: COOK INC VUEOPTIC 150CM FIBER OPTIC BUNDLE; GCJ LAPAROSCOPE, GENERAL & PLASTIC SURGERY

Model Number	N/A
Medical Device Problem Code	Device Operates Differently Than Expected (2913)
Health Effect - Clinical Code	Perforation (2001)
Date of Event	03/31/2017
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).The event is currently under investigation.A follow-up report will be submitted upon receipt of additional information or completion of the investigation.
Event or Problem Description
It was reported that the physician performed a diagnostic ureteroscopy procedure on a patient by using flexor 180 deflecting ureteral access sheath and vueoptic 150cm fiber optic bundle devices together.During the sheath advancement, the physician noticed the ureter was perforated due to larger outer lumen of the flexor 180 deflecting ureteral access sheath and lack of appropriate flexion.No section of the device remained inside the patient¿s body.The physician was unable to complete the procedure.A stent and repeat diagnostic urs was scheduled for the patient.This med watch report is for vueoptic 150cm fiber optic bundle.Please see mdr # 1820334-2017-00675 for the second device (flexor 180 deflecting ureteral access sheath) used on this patient.
Additional Manufacturer Narrative
Investigation ¿ evaluation: a review of complaint history, device history record, documentation and specification was conducted during the investigation.The vueoptic 150cm fiber optic bundle was not returned for evaluation and no photos have been provided.Without the complaint device, a physical investigation was not able to be completed.There is no indication that a design or process related failure mode contributed to this event.A review of production and quality documentation did not identify any specific issues with current manufacturing or quality controls that may have contributed to this incident.The device history record was reviewed and no non-conformances were noted.A review of complaint history revealed two additional complaints associated with complaint lot number 5346681.All three complaints are from the same customer.The three complaints from this customer for this device/lot number combination have been captured in mfr.Report numbers 1820334-2017-00835, 1820334-2017-00887, and 1820334-2017-00889.Based on the investigation evaluation the actual root cause is unknown and no conclusion can be drawn.Per the quality engineering risk assessment, no further action is required.Cook medical has notified the appropriate personnel and will continue to monitor this device via the complaints database for similar complaints.

• Brand Name: VUEOPTIC 150CM FIBER OPTIC BUNDLE
• Common Device Name: GCJ LAPAROSCOPE, GENERAL & PLASTIC SURGERY
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• MDR Report Key: 6537391
• Report Number: 1820334-2017-00887
• Device Sequence Number: 1659077
• Product Code: GCJ
• UDI-Device Identifier: 00827002253438
• UDI-Public: (01)00827002253438(17)171008(10)5346681
• Combination Product (Y/N): N
• Initial Reporter Country: BC
• PMA/510(K) Number: K072521
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor,foreign,health pr
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 11/13/2017

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: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: FVO-150
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 04/03/2017
• Supplement Date Received by Manufacturer: 10/31/2017
• Initial Report FDA Received Date: 05/02/2017
• Supplement Report FDA Received Date: 11/13/2017
• 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