VITEK 2 GN TEST KIT
Received Nov 22, 2016
Report 1950204-2016-00190 · MDR key 6120952
Device
Product problems
- Incorrect, Inadequate or Imprecise Result or Readings
- Incorrect, Inadequate or Imprecise Result or Readings
Patient
Not reported
- No Known Impact Or Consequence To Patient
- No Known Impact Or Consequence To Patient
Narrative
Additional Manufacturer Narrative
AN INVESTIGATION WAS CONDUCTED FOR A MISIDENTIFICATION OF ESCHERICHIA COLI AS SERRATIA FONTICOLA IN ASSOCIATION WITH THE VITEK® 2 GN TEST KIT. INFORMATION SHOWED THE CUSTOMER WAS HAVING IDENTIFICATION ISSUES WITH MULTIPLE SPECIES. TROUBLESHOOTING INDICATED THAT THE CUSTOMER PREPARED THEIR OWN MEDIA, THEIR SALINE MAY HAVE BEEN CONTAMINATED, AND THEY DID NOT TEST ISOLATES AT THE APPROPRIATE AGE OF CULTURE. AFTER THE CUSTOMER USED PREPARED MEDIA FROM BIOMERIEUX, STERILE SALINE, AND AN APPROPRIATE AGE OF CULTURE, ALL THE IDENTIFICATION ISSUES CEASED. TWO LAB REPORTS WERE SUBMITTED FOR REVIEW. ONE LAB REPORT SHOWED AN EXCELLENT IDENTIFICATION OF SERRATIA FONTICOLA. THERE WERE FOUR (4) ATYPICAL POSITIVE REACTIONS (ADO, PLE, SAC, DTAG) AGAINST IDENTIFICATION OF E. COLI ACCORDING TO THE GN KNOWLEDGE BASE. THE SECOND LAB REPORT SHOWED AN EXCELLENT IDENTIFICATION OF E. COLI. A REVIEW OF QUALITY RECORDS CONFIRMED GN LOT 241390240 MET FINAL RELEASE CRITERIA AND THERE WERE NO ISSUES WITH INITIAL PERFORMANCE TESTING AN INCREASED NUMBER OF ATYPICAL POSITIVE REACTIONS CAN INDICATE CONTAMINATION, MIXED CULTURE, USE OF NON-RECOMMENDED MEDIA OR OTHER USER SET UP ERRORS OR AN ATYPICAL STRAIN. HOWEVER WITHOUT THE STRAIN, OR RAW DATA IT'S NOT POSSIBLE TO FURTHER EVALUATE THE CAUSE OF THE MISIDENTIFICATION.
Description of Event or Problem
A CUSTOMER IN (B)(6) NOTIFIED BIOMÉRIEUX OF A MISIDENTIFICATION ASSOCIATED WITH THE VITEK 2 GN TEST KIT. THE CUSTOMER REPORTED THE VITEK 2 GN TEST KIT GAVE INADEQUATE RESULTS OF SERRATIA FONTICOLA INSTEAD OF ESCHERICHIA COLI. THE CUSTOMER INDICATED PERFORMING A BIOCHEMICAL MANUAL TEST AS THE ALTERNATE TESTING FOR IDENTIFICATION. THE CUSTOMER INDICATED E. COLI RESULTS WERE REPORTED OUT. AN INTERNAL BIOMÉRIEUX INVESTIGATION WILL BE INITIATED.