inforMED
MalfunctionGKJ

CELL-DYN SMS

Received Nov 16, 2018 · Event occurred Oct 23, 2018

Report 2919069-2018-00056 · MDR key 8081995

Device

Generic name

Automated Blood Film Preparation And Staining

Catalog number

05H29-04

Product problems

  • Sparking
  • Sparking

Patient

Not reported

  • No Code Available
  • No Code Available

Narrative

Additional Manufacturer Narrative

AN EVALUATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE SUBMITTED WHEN THE EVALUATION IS COMPLETE.

Description of Event or Problem

THE CUSTOMER SAW SPARKING ON THE LEFT BACK PART OF THE CELL-DYN SMS (SLIDE MAKER STAINER) SYSTEM AND OBSERVED ERROR MESSAGE, PRESSURE PUMP FAILED. THE CUSTOMER STATED NO SMOKE OR FIRE (FLAME) WAS SEEN AND NO EXPOSURE OR PERSONAL INJURY OCCURRED.

Additional Manufacturer Narrative

AN ABBOTT FIELD SERVICE ENGINEER WAS DISPATCHED TO THE ACCOUNT AND FOUND THE PRESSURE PUMP FUSE WAS BLOWN [FUSE FAST 1A 250V 5X20MM PART 8510020801]. THE SPARKING FROM THE EQUIPMENT WAS LIMITED TO THIS PART AND DID NOT SPREAD TO OTHER PARTS OF THE EQUIPMENT. AFTER THE FUSE WAS REPLACED, THE ANALYZER WAS RETURNED TO NORMAL OPERATION. EVALUATION OF THE CUSTOMER ISSUE INCLUDED A REVIEW OF THE COMPLAINT TEXT, A SEARCH FOR SIMILAR COMPLAINTS, AND A REVIEW OF LABELING. THE REPLACED FUSE IS INTENDED TO PROTECT THE PRESSURE PUMP FROM EXCESSIVE CURRENT AND PERFORMED AS INTENDED. NO RETURNS WERE MADE AVAILABLE FROM THE CUSTOMER SITE FOR THIS EVALUATION. NO SUBSEQUENT REPORTS OF SPARKING ISSUES WERE IDENTIFIED. NO ADVERSE TREND OR SYSTEMATIC ISSUE WAS IDENTIFIED FOR THE ISSUE IDENTIFIED IN THE COMPLAINT. PRODUCT LABELING WAS REVIEWED AND FOUND TO BE ADEQUATE, AS IT CONTAINS INSTRUCTIONS REGARDING ELECTRICAL SPECIFICATIONS AND REQUIREMENTS, ELECTRICAL HAZARDS, AND OF ELECTRICAL SAFETY FOR THE CELL-DYN SMS SYSTEM OPERATOR'S MANUAL. THE ISSUE WAS RESOLVED THROUGH NORMAL SERVICE PROCEDURES. BASED ON ALL AVAILABLE INFORMATION AND ABBOTT DIAGNOSTICS EVALUATION, NO SYSTEMIC ISSUE WAS IDENTIFIED, AND NO PRODUCT DEFICIENCY WAS FOUND.