QUANTIFERON TB GOLD

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 04 report with the FDA on 2015-05-01 for QUANTIFERON TB GOLD manufactured by Cellestis Limited.

Event Text Entries

[20365692] The patient's attorney claims that the patient (b)(6) was tested and found to be positive for (b)(6) based on the use of a cellestis quantiferon tb gold test. The assumption is the test was performed on a lot of (b)(6) tubes which were recalled by the firm (ref 3003964343-01/28/13-001-r). (b)(6) was put on treatment with (b)(6). The attorney claims that the patient was subsequently found not to be positive for (b)(6). The patient's attorney is claiming that (b)(6)received extensive liver damage as well as other injuries and damages.
Patient Sequence No: 1, Text Type: D, B5


[20527448] As a result of a capa investigation, past legal communication was found that was identified as requiring a medwatch report. Based upon the intended use of the product, if a (b)(6)result is obtained, the physician is advised to repeat the test for confirmation, and in general the results of the screening test are to be taken into consideration with the patient's epidemiological history, current medical status and results of other diagnostic evaluations. The alleged problems reported are the outcome of diagnosis, and subsequent treatment of the pt using (b)(6). Cellestis filed notification of their voluntary recall through the regional fda district recall office on 10/16/2012. Closure of the recall by the fda was received 4/25/2013.
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number3003964343-2015-00003
MDR Report Key4747494
Report Source04
Date Received2015-05-01
Date of Report2015-04-30
Date of Event2012-07-24
Date Added to Maude2015-06-11
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 FDA0
Event Location0
Manufacturer ContactDONNA SOWERS
Manufacturer Street19300 GERMANTOWN RD
Manufacturer CityGERMANTOWN MD 20874
Manufacturer CountryUS
Manufacturer Postal20874
Manufacturer Phone2406867876
Single Use3
Remedial ActionRC
Previous Use Code3
Removal Correction Number3003964343-01/28/13-001-
Event Type3
Type of Report3

Device Details

Brand NameQUANTIFERON TB GOLD
Generic NameNONE
Product CodeNCD
Date Received2015-05-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCELLESTIS LIMITED
Manufacturer AddressCHADSTONE,VICTORIA 3148 AS 3148


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2015-05-01

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.