MAUDE Adverse Event Report: COOK INC BANDER URETERAL DIVERSION STENT SET; GBL CATHETER, URETERAL, GENERAL & PLASTIC SURGERY

Catalog Number 025706-S1

Device Problem Device Contamination with Chemical or Other Material (2944)

Patient Problem No Patient Involvement (2645)

Event Date 05/01/2018

Event Type  malfunction  

Manufacturer Narrative

(b)(4).Pma/510(k) #: preamendment.This report includes information known at this time. a follow-up report will be submitted should additional relevant information become available.

Event Description

It was reported that there was a hair-like substance which was inside the sterilised packaging of the bander ureteral diversion stent set.There were no adverse consequences to the patient as a result of this reported issue.The device did not make contact with the patient.

Manufacturer Narrative

Investigation evaluation: investigation methods used include a review of complaint history, the device history record, quality control data, and a visual inspection of the returned device.One unopened package labeled rpn (b)(4) and label lot number 8650421 was received.Visual examination of the sealed package confirmed a long dark hair like fiber trapped beneath the lid packaging tray.Based on the evidence presented by the sample, this event has been attributed to a packaging event.A review of the device history record found no non-conformances associated with the complaint device lot number.A review of complaint history revealed no other complaints associated with the complaint device lot.Based on the information provided and results of the investigation, the cause of this issue is manufacturing related.Measures have been initiated to address this failure.Cook medical has notified the appropriate personnel and will continue to monitor this device via the complaints database for similar complaints.This report is required by the fda under 21 cfr part 803.This report is based on unconfirmed information submitted by others.Neither the submission of this report nor any statement made in it is intended to be an admission that any cook device is defective or malfunctioned; that a death or serious injury occurred; or that any cook device caused or contributed to; or is likely to cause or contribute to a death or serious injury if a malfunction occurred.

• Brand Name: BANDER URETERAL DIVERSION STENT SET
• Type of Device: GBL CATHETER, URETERAL, GENERAL & PLASTIC SURGERY
• Manufacturer (Section D): COOK INC; 750 daniels way; bloomington IN 47404
• MDR Report Key: 7500437
• MDR Text Key: 107826053
• Report Number: 1820334-2018-01289
• Device Sequence Number: 1
• Product Code: GBL
• UDI-Device Identifier: 00827002168183
• UDI-Public: (01)00827002168183(17)210307(10)8650421
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative,foreig
• Type of Report: Initial,Followup
• Report Date: 06/05/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/09/2018
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Catalogue Number: 025706-S1
• Was Device Available for Evaluation?: Yes
• Date Manufacturer Received: 05/30/2018
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1