MAUDE Adverse Event Report: COOK IRELAND LTD ZIMMON BILIARY STENT; FGE CATHETER, BILIARY, DIAGNOSTIC

Model Number	G21707
Medical Device Problem Code	Difficult to Advance (2920)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	11/12/2018
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Cook ireland ltd (manufacturer) is submitting this report on behalf of cook medical incorporated (cmi)(importer).Exemption number: e2016031.Information pertaining to section g.1 as follows: importer site contact and address: (b)(4) cook medical incorporated (cmi) 1025 acuff road p.O box 4195 bloomington indiana 47402-4195.Importer site establishment registration number: 3005580113.Investigation is still pending, a follow up mdr will be submitted to include investigation conclusions.
Event or Problem Description
This file is being reported based on the fda mdr malfunction precedence "difficult advancement".They tried to put the stent in the bile duct, but the stent could not pass through the stricture in the chd.
Event or Problem Description
This file is being reported based on the fda mdr malfunction precedence "difficult advancement." they tried to put the stent in the bile duct, but the stent could not pass through the stricture in the chd.
Additional Manufacturer Narrative
Cook ireland ltd (manufacturer) is submitting this report on behalf of cook medical incorporated (cmi)(importer).Exemption number: e2016031.Information pertaining to section g.1 as follows: importer site contact and address: (b)(6); cook medical incorporated (cmi), 1025 acuff road, p.O box 4195, bloomington, indiana 47402-4195.Importer site establishment registration number: (b)(4).Lab evaluation: 1 x zso-7-10 of lot # c1526431 was returned to cirl for evaluation.There were no defects highlighted as a result of the lab evaluation the lab evaluation reads the physician used the wrong size sent for the procedure.Engineering have given their evidence based reasons for coming up with this in the lab.Documentand ifu review: a review of manufacturing records for lot # c1526431 did not reveal any discrepancy related to the complaint issue.There is no evidence to suggest that this issue effects the entire lot # c1526431 , a review of the complaints history determined that this failure has not occurred previously with lot # c1526431.It may be noted that according to the instructions for use, (b)(4), a contraindications identified includes an ¿inability to pass wireguide or stent through obstructed area¿ and the user is also instructed to: ¿visually inspect with particular attention to kinks, bends and breaks.If any abnormality is detected that would prohibit proper working condition, do not use.¿ root cause: a definitive root cause for the customer complaint could not be determined as the exact operational conditions of use could not be replicated in the laboratory setting.The possible root cause for this complaint is that the physician didn't choose an appropriate size stent for the application.The incorrect wire-guide was used which may have given an indication as to whether the stricture was too tight for the stent and halted the procedure at that point in time.The wire-guide used in the procedure was 0.025in and the correct wire-guide that should have been used is 0.035in.There is no testing to support the usage of the 0.025in wire-guide.The complaint is confirmed based on the customer testimony.Summary: this complaint is confirmed based on customer testimony.According to the information reported, the patient did not experience any adverse effects due to this occurrence.Complaints of this nature will continue to be monitored for emerging trends.
Additional Manufacturer Narrative
Cook ireland ltd (manufacturer) is submitting this report on behalf of cook medical incorporated (cmi)(importer).Exemption number: e2016031.Information pertaining to section g.1 as follows: importer site contact and address: (b)(6).Cook medical incorporated (cmi), 1025 acuff road, p.O box 4195, bloomington, indiana 47402-4195.Importer site establishment registration number: (b)(4).Investigation is still pending, a follow up mdr will be submitted to include investigation conclusions.
Event or Problem Description
This file is being reported based on the fda mdr malfunction precedence "difficult advancement." they tried to put the stent in the bile duct, but the stent could not pass through the stricture in the chd.

• Brand Name: ZIMMON BILIARY STENT
• Common Device Name: FGE CATHETER, BILIARY, DIAGNOSTIC
• Manufacturer (Section D): COOK IRELAND LTD; o halloran road; limerick
• MDR Report Key: 8149910
• Report Number: 3001845648-2018-00570
• Device Sequence Number: 295279
• Product Code: FGE
• UDI-Device Identifier: 00827002217072
• UDI-Public: (01)00827002217072(17)210801(10)C1526431
• Combination Product (Y/N): N
• Initial Reporter Country: KR
• PMA/510(K) Number: K851962
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 01/08/2019

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 Expiration Date: 08/01/2021
• Device Model Number: G21707
• Device Catalogue Number: ZSO-7-10
• Device Lot Number: C1526431
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/03/2018
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 12/11/2018
• Event Location: Hospital
• Initial Date Received by Manufacturer: 11/14/2018
• Supplement Date Received by Manufacturer: 11/14/2018; 11/14/2018
• Initial Report FDA Received Date: 12/11/2018
• Supplement Report FDA Received Date: 01/08/2019; 02/05/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1