FDA Adverse Event Malfunction Summary report: N

EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - PARTIALLY COVERED

MDR report key: 9149703 · Received October 3, 2019

Report

Report Number
3001845648-2019-00504
Event Type
Malfunction
Date Received
October 3, 2019
Date of Event
September 4, 2019
Report Date
November 28, 2019
Manufacturer
COOK IRELAND LTD
Product Code
ESW
UDI-DI
10827002480312
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

PMA/510(K) #: K162717. INVESTIGATION IS STILL PENDING. A FOLLOW UP MDR WILL BE SUBMITTED TO INCLUDE THE INVESTIGATION CONCLUSIONS. COMPLAINTS OF THIS NATURE WILL CONTINUE TO BE MONITORED FOR POTENTIAL EMERGING TRENDS.

Additional Manufacturer Narrative · 0

PMA/510(K)#: K162717. INVESTIGATION IS STILL PENDING. A FOLLOW UP MDR WILL BE SUBMITTED TO INCLUDE THE INVESTIGATION CONCLUSIONS. COMPLAINTS OF THIS NATURE WILL CONTINUE TO BE MONITORED FOR POTENTIAL EMERGING TRENDS.

Additional Manufacturer Narrative · 0

K162717 - US CLEARANCE NUMBER. DEVICE EVALUATION: THE EVO-20-25-10-E DEVICE OF LOT NUMBER C1604125 INVOLVED IN THIS COMPLAINT WAS RETURNED FOR EVALUATION, WITH ITS ORIGINAL PACKAGING. WITH THE INFORMATION PROVIDED, A PHYSICAL EXAMINATION AND DOCUMENT BASED INVESTIGATION WAS CONDUCTED. LAB EVALUATION: THE DEVICE INVOLVED IN THE COMPLAINT WAS EVALUATED IN THE LABORATORY ON THE 19TH SEPTEMBER 2019. THE RETURNED DEVICE LAB FINDINGS AND OBSERVATIONS CAN BE REFERRED THROUGH THE ATTACHED FILES. THE WHITE TIP WAS FOUND TO BE DETACHED FROM THE CATHETER. FROM ADDITIONAL INFORMATION TO BELOW MENTIONED QUESTIONS - AT WHAT POINT DID THEY NOTICED THAT THE WHITE INNER CATHETER -TIP GOT DETACHED FROM CATHETER? - PLEASE DESCRIBE WHAT HAPPENED STEP-BY-STEP TO HELP US GAIN A BETTER INSIGHT AS TO HOW THE WHITE TIP GOT DETACHED? "DURING INSERTION OF THE STENT SYSTEM ,OVER THE LYING GUIDE WIRE, AT 30CM THE DOCTOR SAW THE WITH TIP SOLVED ." DOCUMENTS REVIEW INCLUDING IFU REVIEW: PRIOR TO DISTRIBUTION ALL EVO-20-25-10-E DEVICES ARE SUBJECTED TO A VISUAL INSPECTION AND FUNCTIONAL CHECKS TO ENSURE DEVICE INTEGRITY. THESE INSPECTIONS AND FUNCTIONAL CHECKS ARE OUTLINED IN INTERNAL PROCEDURES IN PLACE AT CIRL. A REVIEW OF THE MANUFACTURING RECORDS FOR EVO-20-25-10-E DEVICE OF LOT NUMBER C1604125 DID NOT REVEAL ANY DISCREPANCIES THAT COULD HAVE CONTRIBUTED TO THIS ISSUE. THERE IS NO EVIDENCE TO SUGGEST THAT THIS ISSUE AFFECTS THE ENTIRE LOT #C1604125; UPON REVIEW OF COMPLAINTS THIS FAILURE MODE HAS NOT OCCURRED PREVIOUSLY WITH THIS LOT #C1604125. THE INSTRUCTIONS FOR USE IFU0061-5 WHICH ACCOMPANIES THIS DEVICE INSTRUCTS THE USER 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." THERE IS NO EVIDENCE TO SUGGEST THAT THE CUSTOMER DID NOT FOLLOW THE INSTRUCTIONS FOR USE. ROOT CAUSE REVIEW: A DEFINITIVE ROOT CAUSE COULD NOT BE DETERMINED AS THE CIRCUMSTANCES OF USE CANNOT BE REPLICATED IN THE LABORATORY. A POSSIBLE ROOT CAUSE COULD BE THAT THE POTENTIAL DAMAGED COULD HAVE OCCURRED DURING DEVICE PREP WHICH THEN DETERIORATED DURING ADVANCEMENT, SUMMARY: ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE. COMPLAINT IS CONFIRMED AS THE FAILURE WAS VERIFIED IN THE LABORATORY. COMPLAINTS OF THIS NATURE WILL CONTINUE TO BE MONITORED FOR POTENTIAL EMERGING TRENDS.

Description of Event or Problem · 0

THE WHITE GOT DETACHED FROM CATHETER. "AS PER COMPLAINT FORM": THE WHITE INNER CATHETER-TIP GOT DETACHED FROM CATHETER.

Description of Event or Problem · 0

THE WHITE GOT DETACHED FROM CATHETER. "AS PER COMPLAINT FORM": THE WHITE INNER CATHETER-TIP GOT DETACHED FROM CATHETER.

Description of Event or Problem · 0

THE WHITE GOT DETACHED FROM CATHETER. "AS PER COMPLAINT FORM": THE WHITE INNER CATHETER-TIP GOT DETACHED FROM CATHETER. FDA MDR REPORTING REQUIRED: EVENT IS FDA MDR REPORTABLE BASED ON THE DEVICE MALFUNCTION REPORTING PRECEDENCE FOR THIS DEVICE FAMILY FOR THE ISSUE OF ¿TIP SEPARATION'. NO ADVERSE EFFECTS TO THE PATIENT HAVE BEEN REPORTED AS OCCURRING.

Additional Manufacturer Narrative · 1

PMA/510(K) #: K162717. INVESTIGATION IS STILL PENDING. A FOLLOW UP MDR WILL BE SUBMITTED TO INCLUDE THE INVESTIGATION CONCLUSIONS. COMPLAINTS OF THIS NATURE WILL CONTINUE TO BE MONITORED FOR POTENTIAL EMERGING TRENDS.

Description of Event or Problem · 1

THE WHITE GOT DETACHED FROM CATHETER. "AS PER COMPLAINT FORM": THE WHITE INNER CATHETER-TIP GOT DETACHED FROM CATHETER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
948282 EVOLUTION® ESOPHAGEAL CONTROLLED-RELEASE STENT - PARTIALLY COVERED ESW PROSTHESIS, ESOPHAGEAL ESW COOK IRELAND LTD G48031 C1604125 10827002480312

Patients

Seq Age Sex Outcome Treatment
1