VITEK® 2 GN ID TEST KIT
Received Jan 18, 2017
Report 1950204-2017-00013 · MDR key 6262452
Device
Generic name
Vitek® 2 Gn Id Test Card
Manufacturer
Biomerieux, IncCatalog number
21341
Lot number
241373140
Product problems
- Incorrect Or Inadequate Test Results
- Incorrect Or Inadequate Test Results
Patient
Not reported
- No Patient Involvement
- No Patient Involvement
Narrative
Additional Manufacturer Narrative
AN INTERNAL BIOMÉRIEUX INVESTIGATION WAS PERFORMED WITH RESULTS AS FOLLOWS: THE ORGANISM WAS TESTED ON MULTIPLE LOTS OF GN CARDS IN DUPLICATE, INCLUDING FOUR (4) LOTS REPORTED BY CUSTOMERS AND ONE (1) RANDOM GN LOT. THE API 20 E WAS PERFORMED, AS WAS THE VITEK® MS. ON TWO (2) OF THE CUSTOMER LOTS, A LOW DISCRIMINATION CALL OF P. PENNERI / P. HAUSERI WAS OBTAINED. ON THE REMAINING TWO (2) CUSTOMER LOTS TESTED AND THE RANDOM LOT, A LOW DISCRIMINATION CALL OF P. PENNERI / P. PNEUMOTROPICA WAS OBTAINED. API 20 E GAVE A GOOD IDENTIFICATION CALL OF P. VULGARIS GROUP. VITEK® MS GAVE A LOW DISCRIMINATION CALL OF P. PENNERI / P. VULGARIS. SINCE THE ORGANISM IS INDOLE POSITIVE, THE VITEK® MS CALL OF P. VULGARIS WOULD BE CORRECT. A COMPARISON OF REACTION RESULTS FOR CARDS GIVING THE MISIDENTIFICATION CALL OF P. PENNERI / P. HAUSERI AGAINST THE EXPECTED REACTION RESULTS FOR P. VULGARIS REVEALED 3 ATYPICAL NEGATIVE REACTIONS (PLE, ILATK, AGLU). A COMPARISON OF REACTION RESULTS FOR CARDS GIVING THE MISIDENTIFICATION CALL OF P. PENNERI/P. PNEUMOTROPICA AGAINST THE EXPECTED REACTION RESULTS FOR P. VULGARIS REVEALED 4 ATYPICAL NEGATIVE REACTIONS (PROA, PLE, ILATK, AGLU). THIS IS AN ATYPICAL ISOLATE.
Description of Event or Problem
A CUSTOMER FROM THE UNITED STATES REPORTED TO BIOMÉRIEUX A MISIDENTIFICATION OF AN API PROFICIENCY TEST URINE SAMPLE OF PROTEUS VULGARIS, AS PROTEUS PENNERI IN ASSOCIATION WITH THE VITEK® 2 GN ID TEST KIT. THE ORGANISM WAS CULTURED 24-48 HOURS ON BAP/TSAB/BLOOD AGAR, USING MCFARLAND RANGE 0.5-0.63. THE CUSTOMER REPEATED THE TEST WITH AN 18-24 HOUR CULTURE, USING MCFARLAND 0.60 AND 0.57. THE IDENTIFICATION RESULT WAS PROTEUS PENNERI. THE VITEK®2 GN TEST REPORTS AND THE PROFICIENCY RESULTS WERE REQUESTED FROM THE CUSTOMER. AN INTERNAL BIOMÉRIEUX INVESTIGATION WILL BE INITIATED.