FDA Adverse Event Malfunction Summary report: N

CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM

MDR report key: 6570918 · Received May 16, 2017

Report

Report Number
9610612-2017-00246
Event Type
Malfunction
Date Received
May 16, 2017
Date of Event
March 23, 2017
Report Date
June 29, 2017
Manufacturer
AESCULAP AG
Product Code
GEI
PMA / PMN Number
K151696
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

AESCULAP INC. (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF AESCULAP AG (MANUFACTURER). EXEMPTION NUMBER: E2014018. MANUFACTURING SITE EVALUATION: EVALUATION ON-GOING.

Description of Event or Problem · 0

COUNTRY OF COMPLAINT: UNITED KINGDOM. IT WAS REPORTED THAT THE CAIMAN WAS ARCING.

Additional Manufacturer Narrative · 1

USED TEST AND ANALYSIS EQUIPMENT: DIGITAL-CAMERA "(B)(6)". FIRST WE MADE A VISIBLE INSPECTION OF THE JAW. EXCEPT THE BLOOD SOILING AN THE CHARRING WE FOUND NO FURTHER ABNORMITIES. THEN WE CHECKED THE MECHANICAL FUNCTION. THE CLAMPING AND THE CUTTING FUNCTION WORKED WELL. ONE PROBABLE ROOT CAUSE IN CASES LIKE THIS IS A NOT PROPER CLEANING DURING SURGERY, SO THAT CARBONIZED RESIDUES OF BLOOD OR TISSUE INITIATE AN ARC. A FURTHER POSSIBLE ROOT CAUSE IS A DAMAGED INSULATION TONGUE (DISSECTION CLIP). THIS DAMAGE CREATED BY WRONG HANDLING DURING CLEANING THE ELECTRODES. A DAMAGE DURING RF- GENERATOR FAILURES CAN BE EXCLUDED. BECAUSE THERE IS SUSPICION OF A DESIGN RELATED ASPECT TO THE FAILURE, WE HAVE ENTERED THIS FAILURE MODE INTO OUR CORRECTIVE AND PREVENTATIVE ACTIONS SYSTEM SO ARE WORKING ON A SOLUTION. A CAPA FOR IMPROVEMENT AND A BETTER DURABILITY WAS STARTED (700003160).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
350801 CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM ENDOSCOPY GEI AESCULAP AG PL740SU 52298653

Patients

Seq Age Sex Outcome Treatment
1 32 YR Other