COULTER AC T 5DIFF CONTROL PLUS
Received Sep 23, 2011 · Event occurred Mar 31, 2009
Report 1061932-2011-01514 · MDR key 2276810
Device
Product problems
- Fluid/Blood Leak
Patient
UNK
- No Known Impact Or Consequence To Patient
Narrative
Description of Event or Problem
THE CUSTOMER REPORTED THE COULTER AC T 5DIFF CONTROL PLUS (HIGH LEVEL CONTROL VIAL) LEAKED WHILE LYING FLAT ON THE COUNTER TOP. THE CONTROL HAD BEEN PIERCED; HOW MANY TIMES IS UNK. THE POTENTIAL FOR BIOHAZARD EXPOSURE WITH THE REPORTED INCIDENT WAS PRESENT. IN ADDITION, THE CONTROL WAS RUN AND THE RECOVERY RESULTS WERE ELEVATED. THIS WAS NOTED DUE TO INCORRECT CONCENTRATION OF CELL SUSPENSION DUE TO MISSING DILUTING FLUID (LEAK). THERE WAS NO EXPOSURE TO MUCOUS MEMBRANES OR OPEN LESIONS. IT IS UNK IF THE MATERIAL SAFETY DATA SHEET (MSDS) WAS REVIEWED, HOWEVER, IT IS READILY AVAILABLE. NO INJURIES OCCURRED AND MEDICAL ATTENTION WAS NOT SOUGHT AS A RESULT OF THIS EVENT. NO REPORTS OF DEATH OR SERIOUS INJURY, AND NO AFFECT TO OPERATOR SAFETY AS A RESULT OF THIS EVENT. THE PRODUCT WAS REPLACED AND ALL ISSUES WERE RESOLVED.
Additional Manufacturer Narrative
PER LABELING, BECKMAN COULTER, INC. URGES ITS CUSTOMER TO COMPLY WITH ALL NATIONAL HEALTH AND SAFETY STANDARDS SUCH AS THE USE OF BARRIER PROTECTION. THIS MAY INCLUDE, BUT IT IS NOT LIMITED TO, PROTECTIVE EYEWEAR, GLOVES, AND SUITABLE LAB ATTIRE WHEN OPERATING OR MAINTAINING THIS OR ANY OTHER AUTOMATED LAB ANALYZER. THE COULTER AC T 5DIFF CONTROL PLUS IS A HEMATOLOGY QUALITY CONTROL MATERIAL USED TO MONITOR THE PERFORMANCE OF THE COULTER AC T 5DIFF HEMATOLOGY ANALYZERS. PICTURES OF THE VIAL WERE EVALUATED. THE RUBBER PART IN THE CAP OF THE HIGH CONTROL VIAL LEAKED WHEN PIERCED. SERVICE WAS NOT DISPATCH FOR THIS EVENT. BASED ON AVAILABLE INFO, THE ROOT CAUSE COULD NOT BE DETERMINED. THIS REPORTABLE EVENT WAS IDENTIFIED DURING A RETROSPECTIVE REVIEW CONDUCTED BETWEEN (B)(6) 2008 AND (B)(6) 2010 OF COMPLAINTS FOR ADDITIONAL REPORTABLE EVENTS.