Every recall we track for Phadia Ab — 4 in all — plus the complaints and injury reports the public filed about them.
Phadia Ab recalls EliA GBM Wells (Material 14551401) for Phadia 250, 2500, and 5000 devices due to false positive results in certain tests. All lots affected.
Phadia recalls its 1000 model 12-3800-01 due to a liquid sensor error that may cause inaccurate test results. All units with serial numbers are affected.
Phadia Ab recalls EliA RF IgM Well (REF 14-5600-01) due to potential for low assay results. Affected units may lead to inaccurate rheumatoid arthritis testing.
Phadia recalls software version 2.1.4 for Phadia 250 instruments used with EliA assays. Using the OK to All function may cause incorrect sample rejections. Affected users should stop using the software until updated.
