FDA Adverse Event Malfunction Summary report: N

VIDAS® LYME IGG

MDR report key: 7961108 · Received October 12, 2018

Report

Report Number
3002769706-2018-00211
Event Type
Malfunction
Date Received
October 12, 2018
Report Date
March 12, 2019
Manufacturer
BIOMERIEUX SA
Product Code
LSR
PMA / PMN Number
K141133
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

AN INTERNAL INVESTIGATION WAS PERFORMED FOR A FALSE NEGATIVE RESULT IN ASSOCIATION WITH VIDAS® LYME IGG (1006179040). COMPLAINT TRENDING ANALYSIS: FOUR COMPLAINTS FOR THE EXTERNAL QUALITY CONTROL ISSUE ON VIDAS LYG BATCH 1006179040/181125-0 LINKED TO THE ACCURUN QUALITY CONTROL SAMPLE. ONE COMPLAINT FOR SENSITIVITY ISSUE ON VIDAS LYG BATCH 1006179040/181125-0 LINKED TO THE PATIENT CLINICAL CONTEXT. THERE IS NEITHER CAPA NOR NON CONFORMITY LINKED TO THIS ISSUE. QUALITY CONTROL RECORDS: THE ANALYSIS OF THE BATCH HISTORY RECORDS OF VIDAS LYG BATCH 1006179040/181125-0 SHOWED NO ANOMALY DURING THE MANUFACTURING, CONTROL AND PACKAGING PROCESSES. STUDY OF INTERNAL SAMPLES CONTROL CHARTS: THIS ANALYSIS WAS CARRIED OUT ON SIX INTERNAL POSITIVE CONTROLS THAT INCLUDED THREE SAMPLES WITH HIGH TEST VALUES AND THREE SAMPLES WITH TEST VALUES CLOSE TO THE CUT-OFF FOR VIDAS LYG BATCH 181125-0 COMPARED TO THREE OTHER BATCHES (180802-0, 180929-0 AND 190104-0). ALL THE RESULTS WERE WITHIN ACCEPTABLE RANGES AND VIDAS LYG BATCH 1006179040/181125-0 CONFORMED TO THE PRODUCT SPECIFICATIONS. TESTS PERFORMED INTERNALLY: BIOMÉRIEUX TESTED SIX INTERNAL SAMPLES FROM THE ACTIVITY PANEL ON VIDAS LYG BATCH 1006179040/181125-0 COMPARED TO TWO OTHER BATCHES MANUFACTURED USING DIFFERENT RAW MATERIAL. ALTHOUGH, VIDAS LYG BATCH 1006179040/181125-0 GIVES SLIGHTLY LOWER TEST VALUES, ALL THE RESULTS ARE WITHIN THE ACCEPTABLE RANGES. THE CUSTOMER'S ACCURUN SAMPLE GAVE POSITIVE RESULTS (BETWEEN 3.19 AND 4.21 TV) WITH THE THREE VIDAS LYG BATCHES (181125-0, 180929-0 AND 190821-0). TESTING REPRODUCED THE LOWER RESULT OBSERVED BY THE CUSTOMER WITH VIDAS LYG BATCH 1006179040/181125-0. THE PATIENT SAMPLE IDENTIFIED (B)(6) IS POSITIVE WITH VIDAS LYG BATCHES 180929-0 AND 190821-0 BUT CLOSE TO THE CUT-OFF (0.18 TV) WITH A NEGATIVE INTERPRETATION WHEN TESTING WITH VIDAS LYG BATCH 1006179040/181125-0. TESTING REPRODUCED A NEGATIVE RESULT OBSERVED BY THE CUSTOMER WHEN USING VIDAS LYG BATCH 1006179040/181125-0. TESTS PERFORMED BY AN EXTERNAL LABORATORY (BIOMNIS): THE PATIENT SAMPLE (B)(6) GAVE A POSITIVE INTERPRETATION WITH PRESENCE OF BANDS ANTI VLSE, ANTI P41 ET ANTI P18. THE ANALYSIS PERFORMED SHOWED THAT VIDAS LYG BATCH 1006179040/181125-0 WAS IN THE TREND OF THE PARAMETER REGARDING ALL THE REQUIRED CRITERIA. ALTHOUGH VIDAS LYG BATCH 1006179040/181125-0 HAD A TREND TO GIVE LOWER RESULTS, ALL THE RESULTS WERE WITHIN ACCEPTABLE RANGES AND WE DID NOT OBSERVED ANY DEGRADATION OF ITS ACTIVITY COMPARED TO ITS RELEASE.

Description of Event or Problem · 1

A CUSTOMER IN (B)(6) CONTACTED BIOMÉRIEUX TO REPORT THE OCCURRENCE A FALSE NEGATIVE PATIENT RESULT IN ASSOCIATION WITH THE VIDAS® LYME IGG ASSAY (REF. 30320). THE INITIAL RESULT WAS 0.19 (NEGATIVE); REPEAT RESULT WAS 0.26 (POSITIVE). THE CUSTOMER ALSO INDICATED THAT QC IS INCONSISTENT FOR THE LYME IGG ASSAY. THERE IS NO INDICATION OR REPORT FROM THE LABORATORY OR A PHYSICIAN THAT THE DISCREPANT RESULT LED TO ANY ADVERSE EVENT RELATED TO THE PATIENT'S STATE OF HEALTH. BIOMÉRIEUX REQUESTED STRAIN SUBMITTAL FROM THE CUSTOMER. A BIOMÉRIEUX INTERNAL INVESTIGATION HAS BEEN INITIATED. NOTE: REFERENCE 30320 (VIDAS LYME IGG) IS NOT REGISTERED IN THE UNITED STATES. THE U.S. SIMILAR DEVICE IS PRODUCT REFERENCE 417401 (VIDAS LYME IGG II).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
801589 VIDAS® LYME IGG VIDAS® LYME IGG LSR BIOMERIEUX SA 1006179040

Patients

Seq Age Sex Outcome Treatment
1