Phadia Ab
RAPSGATAN 7P, UPPSALA, SE
Registered product codes
30 product codes
Recent MDR events
4 on file
Recalls
5 on file
- Open, ClassifiedJan 24, 2024
Complaints that specific samples produced false positive EliA GBM results. A positive signal was present when these samples were tested for coating-solution reactivity using EliA wells without antigen.
View FDA record ↗ - TerminatedJan 28, 2016
All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA SmDP well lot 0018 may be incorrect and must be considered invalid. Patient samples in complaint investigations caused unspecific signals up to 22 U/ml on EliA SmDP well lot 0018. The nonspecific signals are not caused by anti-Sm antibodies, nor by streptavidin antibodies.
View FDA record ↗ - TerminatedUnknown
We want to inform all Phadia 250 system operators performing EliA Assays not to use the function OK to All in any version of Phadia Prime, up to and including 2.1.4, when rejecting and retesting samples with any EliA assay (the OK function may be used for rejecting single tests and dilution of samples in accordance with product DfU).
View FDA record ↗ - TerminatedUnknown
Potential for reporting low assay results
View FDA record ↗ - TerminatedUnknown
code 7-102 Liquid Sensor Error
View FDA record ↗
Compliance history
Matched by FEI 3002807876.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.