CAIMAN DISP.INSTR.NON ARTICUL.D5/360MM
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
AESCULAP INC. (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF AESCULAP AG (MANUFACTURER). EXEMPTION NUMBER: E2014018. MANUFACTURING SITE EVALUATION: EVALUATION ON-GOING.
COUNTRY OF COMPLAINT: UNITED KINGDOM. IT WAS REPORTED THAT THE CAIMAN WAS ARCING.
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 |