Phadia Ab recalls

5 recalls on record · latest: May 24, 2023

Official U.S. recall history for Phadia Ab, compiled from official government records.

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Phadia Ab recalls EliA GBM Wells, Material Number 14551401, for Phadia 250, 2500, and 5000. In vitro diagnostic

May 24, 2023 · Medical device recalls Moderate risk Complaints that specific samples produced false positive EliA GBM results. A po…

Phadia Ab recalls Phadia" 1000 Model # 12-3800-01 Product Usage: The instrument is fully integrated and automated instrument including so…

July 9, 2019 · Medical device recalls Moderate risk code 7-102 Liquid Sensor Error

Phadia Ab recalls EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measuremen…

May 10, 2019 · Medical device recalls Moderate risk Potential for reporting low assay results

Phadia Ab recalls Phadia Prime software, article number 12-4101-00, as used in combination with the Phadia 250 Instrument, article number…

November 20, 2017 · Medical device recalls Moderate risk We want to inform all Phadia 250 system operators performing EliA Assays not to…

Phadia Ab recalls EliA SmDP Well, Article Number 14-5624-01 Product Usage: EliA SmDP is intended for the in vitro semi-quantitative measu…

December 28, 2015 · Medical device recalls Moderate risk All equivocal and positive results (greater or equal 7 EliA U/ml) on EliA SmDP…