FILMARRAY? FLM1-ASY-0001U

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2017-02-08 for FILMARRAY? FLM1-ASY-0001U manufactured by Biomerieux, Inc..

Event Text Entries

[66835950] A customer from (b)(6) reported a false positive candida parapsilosis for a blood culture in association with the filmarray? Instrument. The positive blood culture had an unusual gram stain (no yeast detected) so the bcid (blood culture identification) panel was used for identification purposes. A subsequent culture was negative for candida, but brevundimonas diminuta was isolated. There was no definite yeast on gram or growth on selective agar. The initial filmarray? Result did not match the clinical presentation therefore, a second aliquot was run on the filmarray? Bcid panel and the result was negative. The patient was not on treatment prior to the blood culture. Fluconazole was administered to the patient based on the initial filmarray? Result and then stopped accordingly. The customer confirmed that there was no adverse impact to the patient from the fluconazole treatment. An internal investigation was conducted. The test run files were analyzed internally to find the root cause for the issue. Review of the quality control records for pouch lot 269016 confirmed the lot met all quality control metrics and criteria. In addition, the pouch lot and the filmarray? Instrument were found to be working within design specifications. The investigation has concluded that the most likely cause(s) are: b. 5. 1) differences in sensitivity between filmarray? And standard culture with a low level organism concentration near the limit of detection. The c. Parapsislosis melt signals observed in the initial run indicates a low level organism concentration is present within the sample. Polymicrobial detections can often be difficult to isolate, especially if the secondary organism is a slow growing yeast. B. 5. 2) contamination during sample testing. While the pouch loading instructions and recommended cleaning steps are sufficient to eliminate contamination the vast majority of the time, it is possible that some microbes could be introduced during any part of the testing process. B. 5. 3) low level pouch anomaly. The history of the filmarray? Bcid product indicates that c. Parapsilosis false positive results have occurred in qc at a very low rate. Low level organism or nucleic acid could have been introduced into the testing reagents during manufacturing. The quality control measures for testing reagents, such as filmarray? Bcid, screen for organism and nucleic acid contamination from a high confidence statistical sampling of each lot of reagents and other kit components. A 100% of very low level or sporadic contamination events may not be detected by this process in every instance. The lot was found to be working within product specifications.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3002769706-2017-00019
MDR Report Key6312609
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2017-02-08
Date of Report2017-02-08
Date Mfgr Received2017-01-09
Date Added to Maude2017-02-08
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactELLEN WELTMER
Manufacturer Street595 ANGLUM ROAD
Manufacturer CityHAZELWOOD MO 63042
Manufacturer CountryUS
Manufacturer Postal63042
Manufacturer Phone3147317301
Manufacturer G1BIOMERIEUX INC.
Manufacturer Street100 RANDOLPHE STREET
Manufacturer CityDURHAM NC 27712
Manufacturer CountryUS
Manufacturer Postal Code27712
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFILMARRAY?
Generic NameFILMARRAY?
Product CodeNSU
Date Received2017-02-08
Model NumberFLM1-ASY-0001U
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBIOMERIEUX, INC.
Manufacturer Address100 RANDOLPHE STREET DURHAM NC 27712 US 27712


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2017-02-08

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